famotidine
Generic: famotidine
Labeler: novadoz pharmaceuticals llcDrug Facts
Product Profile
Brand Name
famotidine
Generic Name
famotidine
Labeler
novadoz pharmaceuticals llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
famotidine 40 mg/1
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72205146
Hyphenated Format
72205-146
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 40 mg/1
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)
Packages (4)
Ingredients (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"}