famotidine

Generic: famotidine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-7013
Product ID 63629-7013_2e1e4581-a001-42fd-98f1-91ce454823ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075805
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 636297013
Hyphenated Format 63629-7013

Supplemental Identifiers

RxCUI
284245 310273
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 ANDA075805 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63629-7013-1)
  • 60 TABLET in 1 BOTTLE (63629-7013-2)
  • 90 TABLET in 1 BOTTLE (63629-7013-3)
  • 10 TABLET in 1 BOTTLE (63629-7013-4)
  • 20 TABLET in 1 BOTTLE (63629-7013-5)
source: ndc

Packages (5)

63629-7013-1 30 TABLET in 1 BOTTLE (63629-7013-1) 63629-7013-2 60 TABLET in 1 BOTTLE (63629-7013-2) 63629-7013-3 90 TABLET in 1 BOTTLE (63629-7013-3) 63629-7013-4 10 TABLET in 1 BOTTLE (63629-7013-4) 63629-7013-5 20 TABLET in 1 BOTTLE (63629-7013-5)

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": "2e1e4581-a001-42fd-98f1-91ce454823ff", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["81f24752-3474-3013-0013-5570c8e7baf7"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-7013-1)", "package_ndc": "63629-7013-1", "marketing_start_date": "20050314"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-7013-2)", "package_ndc": "63629-7013-2", "marketing_start_date": "20070626"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-7013-3)", "package_ndc": "63629-7013-3", "marketing_start_date": "20070716"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (63629-7013-4)", "package_ndc": "63629-7013-4", "marketing_start_date": "20101214"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63629-7013-5)", "package_ndc": "63629-7013-5", "marketing_start_date": "20130204"}], "brand_name": "Famotidine", "product_id": "63629-7013_2e1e4581-a001-42fd-98f1-91ce454823ff", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "63629-7013", "generic_name": "Famotidine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075805", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}