Package 43063-668-30

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 43063-668-30
Digits Only 4306366830
Product NDC 43063-668
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)

Marketing

Marketing Status
Discontinued 2026-03-31
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": "413a01b0-e265-c70e-e063-6394a90aac5d", "openfda": {"upc": ["0343063676103"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["30886aaa-4834-4a06-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)", "package_ndc": "43063-668-30", "marketing_end_date": "20260331", "marketing_start_date": "20160415"}], "brand_name": "Sildenafil", "product_id": "43063-668_413a01b0-e265-c70e-e063-6394a90aac5d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "43063-668", "generic_name": "Sildenafil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA078380", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20130531"}