Package 0093-5517-98

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 0093-5517-98
Digits Only 0093551798
Product NDC 0093-5517
Product ID 0093-5517_dc1607a4-e925-4265-b498-53c3936cddb7
Description

90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)

Marketing

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

Linked Drug Pages (1)

Sildenafil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc1607a4-e925-4265-b498-53c3936cddb7", "openfda": {"upc": ["0300935517988"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["2582414d-0ef3-403e-84e8-1d6c812e7eb1"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)", "package_ndc": "0093-5517-98", "marketing_end_date": "20260331", "marketing_start_date": "20130531"}], "brand_name": "Sildenafil", "product_id": "0093-5517_dc1607a4-e925-4265-b498-53c3936cddb7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0093-5517", "generic_name": "Sildenafil", "labeler_name": "Teva Pharmaceuticals USA, 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"}