tamoxifen citrate

Generic: tamoxifen citrate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamoxifen citrate
Generic Name tamoxifen citrate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tamoxifen citrate 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0485
Product ID 50090-0485_84ab39d0-259a-4937-8c47-5924824533c5
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 500900485
Hyphenated Format 50090-0485

Supplemental Identifiers

RxCUI
198240
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
  • 60 TABLET in 1 BOTTLE (50090-0485-1)
source: ndc

Packages (1)

50090-0485-1 60 TABLET in 1 BOTTLE (50090-0485-1)

Ingredients (1)

tamoxifen citrate (10 mg/1)

Linked Drug Pages (1)

Tamoxifen Citrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "84ab39d0-259a-4937-8c47-5924824533c5", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["198240"], "spl_set_id": ["8d731e7e-3b04-49a2-a0f6-3779422174cc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-0485-1)", "package_ndc": "50090-0485-1", "marketing_start_date": "20160629"}], "brand_name": "Tamoxifen Citrate", "product_id": "50090-0485_84ab39d0-259a-4937-8c47-5924824533c5", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50090-0485", "generic_name": "Tamoxifen Citrate", "labeler_name": "A-S Medication Solutions", "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"}