famotidine

Generic: famotidine

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 40 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-146
Product ID 72205-146_34acb853-6632-49cd-970a-e6fd840852d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217400
Listing Expiration 2026-12-31
Marketing Start 2024-08-06

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 72205146
Hyphenated Format 72205-146

Supplemental Identifiers

RxCUI
284245 310273
UPC
0372205146990 0372205145504 0372205145054 0372205146051 0372205145306 0372205145986 0372205145917 0372205146914 0372205145993 0372205146303
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 ANDA217400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (72205-146-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72205-146-30)
  • 100 TABLET, FILM COATED in 1 BOTTLE (72205-146-91)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72205-146-99)
source: ndc

Packages (4)

Ingredients (1)

famotidine (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34acb853-6632-49cd-970a-e6fd840852d3", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0372205146990", "0372205145504", "0372205145054", "0372205146051", "0372205145306", "0372205145986", "0372205145917", "0372205146914", "0372205145993", "0372205146303"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["74a24590-a0b6-4607-8e67-9fadce53389b"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72205-146-05)", "package_ndc": "72205-146-05", "marketing_start_date": "20240918"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-146-30)", "package_ndc": "72205-146-30", "marketing_start_date": "20240918"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72205-146-91)", "package_ndc": "72205-146-91", "marketing_start_date": "20240918"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72205-146-99)", "package_ndc": "72205-146-99", "marketing_start_date": "20240918"}], "brand_name": "Famotidine", "product_id": "72205-146_34acb853-6632-49cd-970a-e6fd840852d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "72205-146", "generic_name": "Famotidine", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA217400", "marketing_category": "ANDA", "marketing_start_date": "20240806", "listing_expiration_date": "20261231"}