famotidine

Generic: famotidine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6582
Product ID 50090-6582_19dcbba7-ac41-459f-9a13-3d9426f44f73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215630
Listing Expiration 2026-12-31
Marketing Start 2022-07-08

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 500906582
Hyphenated Format 50090-6582

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 ANDA215630 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6582-0)
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)
source: ndc

Packages (4)

50090-6582-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6582-0) 50090-6582-1 20 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1) 50090-6582-2 60 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2) 50090-6582-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)

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": "19dcbba7-ac41-459f-9a13-3d9426f44f73", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["3c32f8e2-f54a-422d-9c25-68692ea09001"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6582-0)", "package_ndc": "50090-6582-0", "marketing_start_date": "20230809"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1)", "package_ndc": "50090-6582-1", "marketing_start_date": "20230809"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2)", "package_ndc": "50090-6582-2", "marketing_start_date": "20230809"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)", "package_ndc": "50090-6582-3", "marketing_start_date": "20230809"}], "brand_name": "FAMOTIDINE", "product_id": "50090-6582_19dcbba7-ac41-459f-9a13-3d9426f44f73", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "50090-6582", "generic_name": "FAMOTIDINE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA215630", "marketing_category": "ANDA", "marketing_start_date": "20220708", "listing_expiration_date": "20261231"}