Package 59762-0033-3

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 59762-0033-3
Digits Only 5976200333
Product NDC 59762-0033
Description

300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)

Marketing

Marketing Status
Discontinued 2026-07-31
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": "c1cc0357-ac81-40b6-a401-dfd941495be5", "openfda": {"upc": ["0359762003317"], "unii": ["BW9B0ZE037"], "rxcui": ["577033", "1307427"], "spl_set_id": ["56a962e8-de00-4a97-8904-0b1bd217dd83"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)", "package_ndc": "59762-0033-3", "marketing_end_date": "20260731", "marketing_start_date": "20201109"}], "brand_name": "Sildenafil", "product_id": "59762-0033_c1cc0357-ac81-40b6-a401-dfd941495be5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "59762-0033", "generic_name": "sildenafil", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "NDA021845", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260731", "marketing_start_date": "20120927"}