Package 0378-0144-91

Brand: tamoxifen citrate

Generic: tamoxifen citrate
NDC Package

Package Facts

Identity

Package NDC 0378-0144-91
Digits Only 0378014491
Product NDC 0378-0144
Product ID 0378-0144_2c1fe025-1eb2-4b2f-b8c9-5d0cfc3c683e
Description

60 TABLET in 1 BOTTLE (0378-0144-91)

Marketing

Marketing Status
Marketed Since 2004-02-20
Brand tamoxifen citrate
Generic tamoxifen citrate
Sample Package No

Linked Drug Pages (1)

Tamoxifen Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c1fe025-1eb2-4b2f-b8c9-5d0cfc3c683e", "openfda": {"unii": ["7FRV7310N6"], "rxcui": ["198240", "313195"], "spl_set_id": ["7ee3d3d2-85d1-4018-8e70-5ed8a64ae1f0"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (0378-0144-91)", "package_ndc": "0378-0144-91", "marketing_start_date": "20040220"}], "brand_name": "Tamoxifen Citrate", "product_id": "0378-0144_2c1fe025-1eb2-4b2f-b8c9-5d0cfc3c683e", "dosage_form": "TABLET", "pharm_class": ["Estrogen Agonist/Antagonist [EPC]", "Selective Estrogen Receptor Modulators [MoA]"], "product_ndc": "0378-0144", "generic_name": "Tamoxifen Citrate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamoxifen Citrate", "active_ingredients": [{"name": "TAMOXIFEN CITRATE", "strength": "10 mg/1"}], "application_number": "ANDA074732", "marketing_category": "ANDA", "marketing_start_date": "20030220", "listing_expiration_date": "20261231"}