acid reducer complete
Generic: famotidine, calcium carbonate, magnesium hydroxide
Labeler: walgreen companyDrug Facts
Product Profile
Brand Name
acid reducer complete
Generic Name
famotidine, calcium carbonate, magnesium hydroxide
Labeler
walgreen company
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
calcium carbonate 800 mg/1, famotidine 10 mg/1, magnesium hydroxide 165 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0713
Product ID
0363-0713_2f05da32-f5b0-45a7-92e7-e31132f36a8a
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077355
Listing Expiration
2027-12-31
Marketing Start
2016-01-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630713
Hyphenated Format
0363-0713
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
acid reducer complete (source: ndc)
Generic Name
famotidine, calcium carbonate, magnesium hydroxide (source: ndc)
Application Number
ANDA077355 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
- 10 mg/1
- 165 mg/1
Packaging
- 50 TABLET, CHEWABLE in 1 BOTTLE (0363-0713-71)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2f05da32-f5b0-45a7-92e7-e31132f36a8a", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["H0G9379FGK", "5QZO15J2Z8", "NBZ3QY004S"], "rxcui": ["283641"], "spl_set_id": ["6f1dcfda-c12a-4c3b-80a2-c9e15517c88f"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, CHEWABLE in 1 BOTTLE (0363-0713-71)", "package_ndc": "0363-0713-71", "marketing_start_date": "20160129"}], "brand_name": "Acid Reducer Complete", "product_id": "0363-0713_2f05da32-f5b0-45a7-92e7-e31132f36a8a", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0363-0713", "generic_name": "Famotidine, Calcium Carbonate, Magnesium Hydroxide", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acid Reducer Complete", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "800 mg/1"}, {"name": "FAMOTIDINE", "strength": "10 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "165 mg/1"}], "application_number": "ANDA077355", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20271231"}