Package 68071-4808-3

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 68071-4808-3
Digits Only 6807148083
Product NDC 68071-4808
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4808-3)

Marketing

Marketing Status
Marketed Since 2019-03-20
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1adc9a8a-2ca0-5970-e063-6394a90a09e8", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0368071480832"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["8488cd17-365c-701c-e053-2991aa0af5f9"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4808-3)", "package_ndc": "68071-4808-3", "marketing_start_date": "20190320"}], "brand_name": "Finasteride", "product_id": "68071-4808_1adc9a8a-2ca0-5970-e063-6394a90a09e8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "68071-4808", "generic_name": "Finasteride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA203687", "marketing_category": "ANDA", "marketing_start_date": "20140920", "listing_expiration_date": "20261231"}