famotidine

Generic: famotidine

Labeler: contract pharmacal corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler contract pharmacal corp.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Contract Pharmacal Corp.

Identifiers & Regulatory

Product NDC 10267-5689
Product ID 10267-5689_1c656b34-6eeb-cc3f-e063-6294a90ad3f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217669
Listing Expiration 2026-12-31
Marketing Start 2024-08-31

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 102675689
Hyphenated Format 10267-5689

Supplemental Identifiers

RxCUI
284245 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 ANDA217669 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (10267-5689-1)
  • 1000 TABLET, COATED in 1 BOTTLE (10267-5689-4)
  • 500 TABLET, COATED in 1 BOTTLE (10267-5689-5)
source: ndc

Packages (3)

10267-5689-1 100 TABLET, COATED in 1 BOTTLE (10267-5689-1) 10267-5689-4 1000 TABLET, COATED in 1 BOTTLE (10267-5689-4) 10267-5689-5 500 TABLET, COATED in 1 BOTTLE (10267-5689-5)

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": "1c656b34-6eeb-cc3f-e063-6294a90ad3f8", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["273deac8-c2b0-423f-8662-4f16d91df216"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Contract Pharmacal Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (10267-5689-1)", "package_ndc": "10267-5689-1", "marketing_start_date": "20240831"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (10267-5689-4)", "package_ndc": "10267-5689-4", "marketing_start_date": "20240831"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (10267-5689-5)", "package_ndc": "10267-5689-5", "marketing_start_date": "20240831"}], "brand_name": "Famotidine", "product_id": "10267-5689_1c656b34-6eeb-cc3f-e063-6294a90ad3f8", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "10267-5689", "generic_name": "Famotidine", "labeler_name": "Contract Pharmacal Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217669", "marketing_category": "ANDA", "marketing_start_date": "20240831", "listing_expiration_date": "20261231"}