tamoxifen citrate
Generic: tamoxifen citrate
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
tamoxifen citrate
Generic Name
tamoxifen citrate
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
tamoxifen citrate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5254
Product ID
68071-5254_1d78d7d4-4388-eab7-e063-6394a90a9e7f
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
680715254
Hyphenated Format
68071-5254
Supplemental Identifiers
RxCUI
UPC
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
ANDA070929 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68071-5254-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d78d7d4-4388-eab7-e063-6394a90a9e7f", "openfda": {"upc": ["0368071525434"], "unii": ["7FRV7310N6"], "rxcui": ["198240"], "spl_set_id": ["a5615dbb-3c5e-6ccc-e053-2995a90ab698"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5254-3)", "package_ndc": "68071-5254-3", "marketing_start_date": "20200511"}], "brand_name": "Tamoxifen Citrate", "product_id": "68071-5254_1d78d7d4-4388-eab7-e063-6394a90a9e7f", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "68071-5254", "generic_name": "Tamoxifen Citrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "10 mg/1"}], "application_number": "ANDA070929", "marketing_category": "ANDA", "marketing_start_date": "20110815", "listing_expiration_date": "20261231"}