famotidine

Generic: famotidine

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
direct rx

Identifiers & Regulatory

Product NDC 72189-141
Product ID 72189-141_2be91ea1-1f27-d635-e063-6294a90a4dd1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078916
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

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 72189141
Hyphenated Format 72189-141

Supplemental Identifiers

RxCUI
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 ANDA078916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (72189-141-60)
  • 90 TABLET in 1 BOTTLE (72189-141-90)
source: ndc

Packages (2)

72189-141-60 60 TABLET in 1 BOTTLE (72189-141-60) 72189-141-90 90 TABLET in 1 BOTTLE (72189-141-90)

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": "2be91ea1-1f27-d635-e063-6294a90a4dd1", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["b1b82d2a-cdb5-3e22-e053-2995a90a917d"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-141-60)", "package_ndc": "72189-141-60", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-141-90)", "package_ndc": "72189-141-90", "marketing_start_date": "20201015"}], "brand_name": "FAMOTIDINE", "product_id": "72189-141_2be91ea1-1f27-d635-e063-6294a90a4dd1", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72189-141", "generic_name": "FAMOTIDINE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA078916", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}