famotidine

Generic: famotidine

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler redpharm drug
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2186
Product ID 67296-2186_44f3f815-5d8e-4bc6-e063-6394a90aa4d7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217400
Listing Expiration 2026-12-31
Marketing Start 2024-08-06

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 672962186
Hyphenated Format 67296-2186

Supplemental Identifiers

RxCUI
310273
UPC
0372205146990 0372205145504 0372205145054 0372205146051 0372205145306 0372205145986 0372205145917 0372205146914 0372205145993 0372205146303
UNII
5QZO15J2Z8
NUI
N0000000151 N0000175784

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 famotidine (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA217400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)
source: ndc

Packages (1)

67296-2186-3 30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44f3f815-5d8e-4bc6-e063-6394a90aa4d7", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0372205146990", "0372205145504", "0372205145054", "0372205146051", "0372205145306", "0372205145986", "0372205145917", "0372205146914", "0372205145993", "0372205146303"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["44f3f63d-4522-91e4-e063-6394a90a6d1b"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)", "package_ndc": "67296-2186-3", "marketing_start_date": "20240918"}], "brand_name": "Famotidine", "product_id": "67296-2186_44f3f815-5d8e-4bc6-e063-6394a90aa4d7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67296-2186", "generic_name": "Famotidine", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217400", "marketing_category": "ANDA", "marketing_start_date": "20240806", "listing_expiration_date": "20261231"}