Package 43598-303-90

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 43598-303-90
Digits Only 4359830390
Product NDC 43598-303
Description

90 TABLET, FILM COATED in 1 BOTTLE (43598-303-90)

Marketing

Marketing Status
Marketed Since 2012-10-25
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": "8e1e332b-310c-a528-339a-702c542d14dd", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["c8ed59a3-c5b2-3156-b781-5e514b79011b"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Dr Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-303-30)", "package_ndc": "43598-303-30", "marketing_start_date": "20121025"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43598-303-90)", "package_ndc": "43598-303-90", "marketing_start_date": "20121025"}], "brand_name": "Finasteride", "product_id": "43598-303_8e1e332b-310c-a528-339a-702c542d14dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "43598-303", "generic_name": "Finasteride", "labeler_name": "Dr Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA090061", "marketing_category": "ANDA", "marketing_start_date": "20121025", "listing_expiration_date": "20261231"}