heartburn relief original strength

Generic: famotidine

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heartburn relief original strength
Generic Name famotidine
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-5529
Product ID 0904-5529_4bbca900-8593-427c-8595-c5c6c3456967
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075400
Listing Expiration 2027-12-31
Marketing Start 2009-09-09

Pharmacologic Class

Established (EPC)
histamine-2 receptor antagonist [epc]
Mechanism of Action
histamine h2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09045529
Hyphenated Format 0904-5529

Supplemental Identifiers

RxCUI
199047
UNII
5QZO15J2Z8
NUI
N0000000151 N0000175784

Packaging Origin

Original Packager
true

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 heartburn relief original strength (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA075400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0904-5529-52) / 60 TABLET, FILM COATED in 1 BOTTLE
  • 30 BLISTER PACK in 1 CARTON (0904-5529-87) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

0904-5529-52 1 BOTTLE in 1 CARTON (0904-5529-52) / 60 TABLET, FILM COATED in 1 BOTTLE 0904-5529-87 30 BLISTER PACK in 1 CARTON (0904-5529-87) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

famotidine (10 mg/1)

Linked Drug Pages (1)

heartburn relief original strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bbca900-8593-427c-8595-c5c6c3456967", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["be275c48-18bf-45f6-891d-36d89327813e"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-5529-52)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-5529-52", "marketing_start_date": "20090909"}, {"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-5529-87)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-5529-87", "marketing_start_date": "20090909"}], "brand_name": "heartburn relief original strength", "product_id": "0904-5529_4bbca900-8593-427c-8595-c5c6c3456967", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0904-5529", "generic_name": "Famotidine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "heartburn relief", "brand_name_suffix": "original strength", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA075400", "marketing_category": "ANDA", "marketing_start_date": "20090909", "listing_expiration_date": "20271231"}