famotidine

Generic: famotidine

Labeler: walgreen co.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler walgreen co.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
WALGREEN CO.

Identifiers & Regulatory

Product NDC 0363-1899
Product ID 0363-1899_f1138f9a-9f0a-46ee-b1de-ee1baea25269
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206531
Listing Expiration 2026-12-31
Marketing Start 2022-02-18

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 03631899
Hyphenated Format 0363-1899

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 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 (0363-1899-14) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1899-24) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1899-34) / 200 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1899-53) / 25 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f1138f9a-9f0a-46ee-b1de-ee1baea25269", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["d0f74e78-7afb-49c2-e053-2a95a90a31dc"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["WALGREEN CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1899-14)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1899-14", "marketing_start_date": "20220218"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1899-24)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1899-24", "marketing_start_date": "20220218"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1899-34)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1899-34", "marketing_start_date": "20220218"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1899-53)  / 25 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1899-53", "marketing_start_date": "20220218"}], "brand_name": "Famotidine", "product_id": "0363-1899_f1138f9a-9f0a-46ee-b1de-ee1baea25269", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0363-1899", "generic_name": "Famotidine", "labeler_name": "WALGREEN CO.", "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": "20220218", "listing_expiration_date": "20261231"}