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 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0942
Product ID 50090-0942_7bfc1a17-2123-4f1b-bde7-cd6763ec10da
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 500900942
Hyphenated Format 50090-0942

Supplemental Identifiers

RxCUI
313195
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
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (50090-0942-0)
source: ndc

Packages (1)

50090-0942-0 90 TABLET in 1 BOTTLE, PLASTIC (50090-0942-0)

Ingredients (1)

tamoxifen citrate (20 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": "7bfc1a17-2123-4f1b-bde7-cd6763ec10da", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["313195"], "spl_set_id": ["716657e8-d809-4671-87bc-8d10ef69a071"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (50090-0942-0)", "package_ndc": "50090-0942-0", "marketing_start_date": "20141128"}], "brand_name": "Tamoxifen Citrate", "product_id": "50090-0942_7bfc1a17-2123-4f1b-bde7-cd6763ec10da", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "50090-0942", "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": "20 mg/1"}], "application_number": "ANDA070929", "marketing_category": "ANDA", "marketing_start_date": "20110815", "listing_expiration_date": "20261231"}