famotidine
Generic: famotidine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
famotidine
Generic Name
famotidine
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
famotidine 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0370
Product ID
71335-0370_337a85de-6910-03aa-e063-6294a90a2e71
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206530
Listing Expiration
2026-12-31
Marketing Start
2015-12-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350370
Hyphenated Format
71335-0370
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA206530 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
- 50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)
Packages (8)
71335-0370-1
30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)
71335-0370-2
60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)
71335-0370-3
20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)
71335-0370-4
90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)
71335-0370-5
100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
71335-0370-6
10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
71335-0370-7
120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
71335-0370-8
50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "337a85de-6910-03aa-e063-6294a90a2e71", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["11ce2a78-76ce-44df-afe3-57493498e596"], "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, FILM COATED in 1 BOTTLE (71335-0370-1)", "package_ndc": "71335-0370-1", "marketing_start_date": "20210416"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)", "package_ndc": "71335-0370-2", "marketing_start_date": "20210723"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)", "package_ndc": "71335-0370-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)", "package_ndc": "71335-0370-4", "marketing_start_date": "20210504"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)", "package_ndc": "71335-0370-5", "marketing_start_date": "20211227"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)", "package_ndc": "71335-0370-6", "marketing_start_date": "20210629"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)", "package_ndc": "71335-0370-7", "marketing_start_date": "20210902"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)", "package_ndc": "71335-0370-8", "marketing_start_date": "20211227"}], "brand_name": "Famotidine", "product_id": "71335-0370_337a85de-6910-03aa-e063-6294a90a2e71", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71335-0370", "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": "ANDA206530", "marketing_category": "ANDA", "marketing_start_date": "20151222", "listing_expiration_date": "20261231"}