Package 0591-4050-94

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 0591-4050-94
Digits Only 0591405094
Product NDC 0591-4050
Description

1 BOTTLE in 1 CARTON (0591-4050-94) / 112 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-08-17
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": "4c7d4ea0-d3b7-4a20-b5d6-09207153aaad", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["0e6428c0-e0e9-4fc0-8615-6a9678d2286c"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0591-4050-94)  / 112 mL in 1 BOTTLE", "package_ndc": "0591-4050-94", "marketing_start_date": "20200817"}], "brand_name": "Sildenafil", "product_id": "0591-4050_4c7d4ea0-d3b7-4a20-b5d6-09207153aaad", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0591-4050", "generic_name": "Sildenafil", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA211534", "marketing_category": "ANDA", "marketing_start_date": "20200817", "listing_expiration_date": "20261231"}