Package 0904-6019-46

Brand: bicalutamide

Generic: bicalutamide
NDC Package

Package Facts

Identity

Package NDC 0904-6019-46
Digits Only 0904601946
Product NDC 0904-6019
Description

30 TABLET in 1 BOTTLE (0904-6019-46)

Marketing

Marketing Status
Discontinued 2026-03-31
Brand bicalutamide
Generic bicalutamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8ac6fd8c-6c02-4bd1-8e19-ab1a6ce4b9c1", "openfda": {"nui": ["N0000000243", "N0000175560"], "unii": ["A0Z3NAU9DP"], "rxcui": ["199123"], "spl_set_id": ["82d4877e-6ebf-4f75-a108-28dc840b07fc"], "pharm_class_epc": ["Androgen Receptor Inhibitor [EPC]"], "pharm_class_moa": ["Androgen Receptor Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0904-6019-46)", "package_ndc": "0904-6019-46", "marketing_end_date": "20260331", "marketing_start_date": "20100511"}], "brand_name": "Bicalutamide", "product_id": "0904-6019_8ac6fd8c-6c02-4bd1-8e19-ab1a6ce4b9c1", "dosage_form": "TABLET", "pharm_class": ["Androgen Receptor Antagonists [MoA]", "Androgen Receptor Inhibitor [EPC]"], "product_ndc": "0904-6019", "generic_name": "Bicalutamide", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bicalutamide", "active_ingredients": [{"name": "BICALUTAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA078917", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20100511"}