heartburn relief

Generic: famotidine

Labeler: meijer distribution inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heartburn relief
Generic Name famotidine
Labeler meijer distribution inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Meijer Distribution Inc

Identifiers & Regulatory

Product NDC 41250-712
Product ID 41250-712_889e4edf-e58d-4fa4-8ed1-5b4eab8c8e49
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077351
Listing Expiration 2026-12-31
Marketing Start 2019-04-17

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 41250712
Hyphenated Format 41250-712

Supplemental Identifiers

RxCUI
310273
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 (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA077351 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 25 BLISTER PACK in 1 CARTON (41250-712-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (41250-712-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (41250-712-78) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

41250-712-02 25 BLISTER PACK in 1 CARTON (41250-712-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK 41250-712-71 1 BOTTLE in 1 CARTON (41250-712-71) / 50 TABLET, FILM COATED in 1 BOTTLE 41250-712-78 2 BOTTLE in 1 CARTON (41250-712-78) / 50 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

heartburn relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "889e4edf-e58d-4fa4-8ed1-5b4eab8c8e49", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["263ee489-fc3f-4578-b3a5-44f6d7757898"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (41250-712-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "41250-712-02", "marketing_start_date": "20190417"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-712-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-712-71", "marketing_start_date": "20190417"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (41250-712-78)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-712-78", "marketing_start_date": "20220811"}], "brand_name": "heartburn relief", "product_id": "41250-712_889e4edf-e58d-4fa4-8ed1-5b4eab8c8e49", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "41250-712", "generic_name": "famotidine", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "heartburn relief", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20190417", "listing_expiration_date": "20261231"}