tamoxifen citrate

Generic: tamoxifen citrate

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamoxifen citrate
Generic Name tamoxifen citrate
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tamoxifen citrate 10 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

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
estrogen agonist/antagonist [epc] selective estrogen receptor modulators [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680715254
Hyphenated Format 68071-5254

Supplemental Identifiers

RxCUI
198240
UPC
0368071525434
UNII
7FRV7310N6

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-5254-3)
source: ndc

Packages (1)

Ingredients (1)

tamoxifen citrate (10 mg/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"}