famotidine

Generic: famotidine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-781
Product ID 71205-781_fe21daca-ac48-4b46-9cb3-9a69af0c6a84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075511
Listing Expiration 2026-12-31
Marketing Start 2001-04-16

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 71205781
Hyphenated Format 71205-781

Supplemental Identifiers

RxCUI
284245
UPC
0371205781903
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 ANDA075511 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)
source: ndc

Packages (3)

71205-781-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30) 71205-781-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60) 71205-781-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)

Ingredients (1)

famotidine (40 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": "fe21daca-ac48-4b46-9cb3-9a69af0c6a84", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0371205781903"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["fe21daca-ac48-4b46-9cb3-9a69af0c6a84"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)", "package_ndc": "71205-781-30", "marketing_start_date": "20230327"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)", "package_ndc": "71205-781-60", "marketing_start_date": "20230327"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)", "package_ndc": "71205-781-90", "marketing_start_date": "20230327"}], "brand_name": "Famotidine", "product_id": "71205-781_fe21daca-ac48-4b46-9cb3-9a69af0c6a84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71205-781", "generic_name": "Famotidine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA075511", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}