Package 68001-597-05

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68001-597-05
Digits Only 6800159705
Product NDC 68001-597
Description

90 TABLET, FILM COATED in 1 BOTTLE (68001-597-05)

Marketing

Marketing Status
Marketed Since 2023-06-12
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": "28da809a-99b6-e220-e063-6294a90ac8ae", "openfda": {"upc": ["0368001597050", "0368001363051"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["be6d1015-306d-44fb-8d4d-01724b8d9590"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68001-597-05)", "package_ndc": "68001-597-05", "marketing_start_date": "20230612"}], "brand_name": "Sildenafil", "product_id": "68001-597_28da809a-99b6-e220-e063-6294a90ac8ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68001-597", "generic_name": "Sildenafil", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203814", "marketing_category": "ANDA", "marketing_start_date": "20230612", "listing_expiration_date": "20261231"}