famotidine

Generic: famotidine

Labeler: better living brands, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler better living brands, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Better Living Brands, LLC

Identifiers & Regulatory

Product NDC 21130-033
Product ID 21130-033_40a6d1b8-f8bd-4d21-9bde-425d5e9e2c8b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206531
Listing Expiration 2026-12-31
Marketing Start 2023-09-08

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 21130033
Hyphenated Format 21130-033

Supplemental Identifiers

RxCUI
310273
UPC
0321130782452
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 famotidine (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA206531 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (21130-033-14) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-033-34) / 200 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (21130-033-53) / 25 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

21130-033-14 1 BOTTLE in 1 CARTON (21130-033-14) / 50 TABLET, FILM COATED in 1 BOTTLE 21130-033-34 1 BOTTLE in 1 CARTON (21130-033-34) / 200 TABLET, FILM COATED in 1 BOTTLE 21130-033-53 1 BOTTLE in 1 CARTON (21130-033-53) / 25 TABLET, FILM COATED in 1 BOTTLE

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": "40a6d1b8-f8bd-4d21-9bde-425d5e9e2c8b", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0321130782452"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["f6f0230c-44fb-6c36-e053-6394a90ac43e"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-033-14)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-033-14", "marketing_start_date": "20230908"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-033-34)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-033-34", "marketing_start_date": "20230908"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-033-53)  / 25 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "21130-033-53", "marketing_start_date": "20230908"}], "brand_name": "Famotidine", "product_id": "21130-033_40a6d1b8-f8bd-4d21-9bde-425d5e9e2c8b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "21130-033", "generic_name": "Famotidine", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA206531", "marketing_category": "ANDA", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}