tamoxifen citrate
Generic: tamoxifen citrate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tamoxifen citrate
Generic Name
tamoxifen citrate
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
tamoxifen citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2209
Product ID
72162-2209_8222e567-8174-40fc-afd8-ab6bde6dc073
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213358
Listing Expiration
2026-12-31
Marketing Start
2020-08-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622209
Hyphenated Format
72162-2209
Supplemental Identifiers
RxCUI
UNII
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
tamoxifen citrate (source: ndc)
Generic Name
tamoxifen citrate (source: ndc)
Application Number
ANDA213358 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8222e567-8174-40fc-afd8-ab6bde6dc073", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["313195"], "spl_set_id": ["9b4a8abc-6e56-40c5-a826-1d1f3c0786e1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2209-3)", "package_ndc": "72162-2209-3", "marketing_start_date": "20240105"}], "brand_name": "Tamoxifen Citrate", "product_id": "72162-2209_8222e567-8174-40fc-afd8-ab6bde6dc073", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "72162-2209", "generic_name": "Tamoxifen Citrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA213358", "marketing_category": "ANDA", "marketing_start_date": "20200814", "listing_expiration_date": "20261231"}