Drugs Similar to ACID REDUCER

RANITIDINE HYDROCHLORIDE

Related medications based on brand, generic name, substance, active ingredients.

By Brand

Drugs with the same brand name or brand family

Acid Reducer OMEPRAZOLE
7-ELEVEN FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
FAMILY DOLLAR STORES, LLC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
CARDINAL HEALTH FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
DISCOUNT DRUG MART FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
RELIABLE 1 LABORATORIES LLC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
FRED'S, INC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
WALGREEN CO. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
AUROHEALTH LLC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
BEST CHOICE FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
AUROHEALTH LLC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
CVS PHARMACY, INC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
INNOVUS PHARMACEUTICALS, INC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
WINCO FOODS, LLC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
WAL-MART STORES, INC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
RUGBY LABORATORIES FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
KROGER COMPANY FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
AUROHEALTH LLC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
BI-MART FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer OMEPRAZOLE
NORTHEAST PHARMA FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Acid Reducer ESOMEPRAZOLE MAGNESIUM
CVS PHARMACY FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

By Generic Name

Drugs with the same generic name (different brands)

Ranitidine Hydrochloride RANITIDINE HYDROCHLORIDE
DR. REDDY'S LABORATORIES LIMITED FDA Rx Only

Ranitidine hydrochloride (HCl) USP, is a histamine H 2 -receptor antagonist. Chemically it is N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N’-methyl-2-nitro-1,1-ethenediamine, HCl. It has the following structural formula: The molecular formula is C 13 H 22 N 4 O 3 S•HCl, representing a molecular weight of 350.87. Ranitidine hydrochloride USP is a white to pale yellow, crystalline practically odorless powder, is sensitive to light and moisture. It is very soluble in water and sparingly soluble in alcohol. Each Ranitidine Hydrochloride capsule, for oral administration, contains 167.4 mg or 334.8 mg of ranitidine hydrochloride equivalent to 150 mg or 300 mg of ranitidine, respectively. In addition, each capsule contains the following inactive ingredients: Microcrystalline Cellulose, Sodium Starch Glycolate, Magnesium Stearate. The capsule shells contain Black Iron Oxide, Red Iron Oxide T3469, Yellow Iron Oxide T3506, Titanium Dioxide and Gelatin. The capsule shells are imprinted with edible ink.

By Substance

Drugs sharing the same substance name

RANITIDINE RANITIDINE
RISING PHARMA HOLDINGS, INC. FDA Rx Only

Ranitidine Tablets USP are available for oral administration containing 150 mg or 300 mg of ranitidine. The active ingredient in Ranitidine Tablets USP, 150 mg and 300 mg is Ranitidine hydrochloride (HCl), USP, a histamine H 2 -receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl] methyl]thio]ethyl]-N´-methyl-2-nitro-1,1-ethenediamine, HCl. It has the following structure: The emperical formula is C 13 H 22 N 4 O 3 S•HCl, representing a molecular weight of 350.87. Ranitidine HCl is white to pale yellow, crystalline, practically odorless powder, sensitive to light and moisture. Melts at about 140°C with decomposition. Ranitidine is available as 150 mg and 300 mg tablets for oral administration. Each Ranitidine Tablet USP, 150 mg contains 150 mg ranitidine (equivalent to 168 mg of ranitidine HCl) and the following inactive ingredients microcrystalline cellulose, croscarmellose sodium, magnesium stearate, Opadry ® 200 Orange 203A530006 (Polyvinyl alcohol, talc, titanium dioxide, glycerol monostearate, sodium lauryl sulphate, FD&C yellow 6 and iron oxide yellow), purified water. Each Ranitidine Tablet USP, 300 mg contains 300 mg ranitidine (equivalent to 336 mg of ranitidine HCl) and the following inactive ingredients microcrystalline cellulose, croscarmellose sodium, magnesium stearate, Opadry ® 200 Yellow 203A520014 (Polyvinyl alcohol, talc, titanium dioxide, glycerol monostearate, sodium lauryl sulphate, FD&C yellow 5 and FD&C Blue 1), purified water. Contains color additives including FD&C Yellow No.5 (tartrazine) Meets FDA approved specifications for nitrosamine impurities. ranitidine-hcl-struc

Ranitidine RANITIDINE
AJANTA PHARMA USA INC. FDA Rx Only

Ranitidine hydrochloride (HCl) USP, is a histamine H 2 -receptor antagonist. Chemically it is N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N’-methyl-2-nitro-1,1-ethenediamine,hydrochloride. It has the following structure: The empirical formula is C 13 H 22 N 4 O 3 S • HCl, representing a molecular weight of 350.8. Ranitidine HCl is a white to pale yellow crystalline, practically odorless powder. Very soluble in water, sparingly soluble in alcohol. Each capsule, for oral administration contains 168 mg or 336 mg of ranitidine hydrochloride equivalent to 150 mg and 300 mg of ranitidine, respectively. Inactive ingredients: Silicon dioxide, corn starch, magnesium stearate, and sodium starch glycolate Type A corn. Each hard-gelatin capsule contains gelatin, titanium dioxide, FD&C Blue no. 1, FD&C Red no. 40, and FD&C Yellow no. 6. Imprinting ink contains: shellac, propylene glycol, ferrosoferric oxide and potassium hydroxide. structure

Ranitidine RANITIDINE
DR. REDDY'S LABORATORIES LIMITED FDA OTC

Uses relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Ranitidine RANITIDINE
DR. REDDY'S LABORATORIES LIMITED FDA OTC

Use(s) relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Ranitidine RANITIDINE
AMNEAL PHARMACEUTICALS OF NEW YORK LLC FDA Rx Only

The active ingredient in Ranitidine Tablets, USP 150 mg and Ranitidine Tablets, USP 300 mg is ranitidine hydrochloride (HCl), USP, a histamine H 2 -receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine, HCl. It has the following structure: The empirical formula is C 13 H 22 N 4 O 3 S·HCl, representing a molecular weight of 350.87. Ranitidine HCl is a white to pale yellow, granular substance that is soluble in water. It has a slightly bitter taste and sulfurlike odor. Each Ranitidine Tablets, USP 150 mg for oral administration contains 167.4 mg of ranitidine HCl equivalent to 150 mg of ranitidine. Each tablet also contains the inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, titanium dioxide, triethyl citrate and FD&C Yellow #6. Each Ranitidine Tablets, USP 300 mg for oral administration contains 334.8 mg of ranitidine HCl equivalent to 300 mg of ranitidine. Each tablet also contains the inactive ingredients colloidal silicon dioxide, croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, titanium dioxide, triethyl citrate and D&C Yellow #10. Click to Zoom In

Ranitidine, Ranitidine cool mint RANITIDINE
GRANULES INDIA LTD FDA OTC

USE(S) ◾ relieves heartburn associated with acid indigestion and sour stomach ◾ prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Ranitidine Hydrochloride RANITIDINE HYDROCHLORIDE
DR. REDDY'S LABORATORIES LIMITED FDA Rx Only

Ranitidine hydrochloride (HCl) USP, is a histamine H 2 -receptor antagonist. Chemically it is N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N’-methyl-2-nitro-1,1-ethenediamine, HCl. It has the following structural formula: The molecular formula is C 13 H 22 N 4 O 3 S•HCl, representing a molecular weight of 350.87. Ranitidine hydrochloride USP is a white to pale yellow, crystalline practically odorless powder, is sensitive to light and moisture. It is very soluble in water and sparingly soluble in alcohol. Each Ranitidine Hydrochloride capsule, for oral administration, contains 167.4 mg or 334.8 mg of ranitidine hydrochloride equivalent to 150 mg or 300 mg of ranitidine, respectively. In addition, each capsule contains the following inactive ingredients: Microcrystalline Cellulose, Sodium Starch Glycolate, Magnesium Stearate. The capsule shells contain Black Iron Oxide, Red Iron Oxide T3469, Yellow Iron Oxide T3506, Titanium Dioxide and Gelatin. The capsule shells are imprinted with edible ink.

By Active Ingredients

Drugs sharing any active ingredients

Omeprazole OMEPRAZOLE
#7 20 mg
CVS PHARAMACY, INC FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Omeprazole OMEPRAZOLE
#7 20 mg
MEIJER DISTRIBUTION INC. FDA OTC

Use treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

OMEPRAZOLE OMEPRAZOLE
#7 20 mg
AMERISOURCE BERGEN FDA OTC

Uses • treats frequent heartburn (occurs 2 or more days a week) • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

omeprazole OMEPRAZOLE
#7 20 mg
INNOVUS PHARMACEUTICALS, INC. FDA OTC

Use ▪ treats frequent heartburn (occurs 2 or more days a week) ▪ not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

omeprazole OMEPRAZOLE
#7 20 mg
RITE AID FDA OTC

Use ▪ treats frequent heartburn (occurs 2 or more days a week) ▪ not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DR. REDDY'S LABORATORIES INC. FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
WALGREENS COMPANY FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
KROGER COMPANY FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
HEB FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
THE KROGER CO. FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DR. REDDYS LABORATORIES INC FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
CVS PHARMACY FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DR. REDDY'S LABORATORIES INC FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
H E B FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DISCOUNT DRUG MART, INC FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DR. REDDY'S LABORATORIES INC FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
CARDINAL HEALTH FDA OTC

Uses treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
CHAIN DRUG MARKETING ASSOCIATION INC FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
CHAIN DRUG MARKETING ASSOCIATION, INC. FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Esomeprazole Magnesium ESOMEPRAZOLE MAGNESIUM
DR. REDDY'S LABORATORIES INC FDA OTC

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

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