tamoxifen citrate
Generic: tamoxifen citrate
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
tamoxifen citrate
Generic Name
tamoxifen citrate
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Routes
Active Ingredients
tamoxifen citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-2473
Product ID
0591-2473_20254a14-2e07-4279-8263-c63b6a71d861
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070929
Listing Expiration
2026-12-31
Marketing Start
2011-08-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05912473
Hyphenated Format
0591-2473
Supplemental Identifiers
RxCUI
UNII
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
tamoxifen citrate (source: ndc)
Generic Name
tamoxifen citrate (source: ndc)
Application Number
ANDA070929 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (0591-2473-19)
- 30 TABLET in 1 BOTTLE, PLASTIC (0591-2473-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20254a14-2e07-4279-8263-c63b6a71d861", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["198240", "313195"], "spl_set_id": ["9b8a4211-120f-4981-ad69-928accb97637"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (0591-2473-19)", "package_ndc": "0591-2473-19", "marketing_start_date": "20110815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (0591-2473-30)", "package_ndc": "0591-2473-30", "marketing_start_date": "20110815"}], "brand_name": "Tamoxifen Citrate", "product_id": "0591-2473_20254a14-2e07-4279-8263-c63b6a71d861", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "0591-2473", "generic_name": "Tamoxifen Citrate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA070929", "marketing_category": "ANDA", "marketing_start_date": "20110815", "listing_expiration_date": "20261231"}