Package 0093-5342-56

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 0093-5342-56
Digits Only 0093534256
Product NDC 0093-5342
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-5342-56)

Marketing

Marketing Status
Marketed Since 2017-12-11
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f85e5bfc-be48-4675-8867-1585f412ccb6", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["5cbac450-f336-45bd-8d10-9ecfd21866eb"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-5342-01)", "package_ndc": "0093-5342-01", "marketing_start_date": "20171211"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-5342-56)", "package_ndc": "0093-5342-56", "marketing_start_date": "20171211"}], "brand_name": "Sildenafil", "product_id": "0093-5342_f85e5bfc-be48-4675-8867-1585f412ccb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0093-5342", "generic_name": "Sildenafil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA077342", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}