Package 59651-420-11

Brand: sildenafil citrate

Generic: sildenafil citrate
NDC Package

Package Facts

Identity

Package NDC 59651-420-11
Digits Only 5965142011
Product NDC 59651-420
Product ID 59651-420_39509319-16be-4fc4-a60a-48ea8e9333c6
Description

1 BOTTLE in 1 CARTON (59651-420-11) / 112 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-12-23
Brand sildenafil citrate
Generic sildenafil citrate
Sample Package No

Linked Drug Pages (1)

sildenafil CITRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39509319-16be-4fc4-a60a-48ea8e9333c6", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["b60b4fdc-9b78-45e6-8438-8a30f83ed976"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59651-420-11)  / 112 mL in 1 BOTTLE", "package_ndc": "59651-420-11", "marketing_start_date": "20221223"}], "brand_name": "sildenafil CITRATE", "product_id": "59651-420_39509319-16be-4fc4-a60a-48ea8e9333c6", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "59651-420", "generic_name": "sildenafil CITRATE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sildenafil CITRATE", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA214773", "marketing_category": "ANDA", "marketing_start_date": "20221223", "listing_expiration_date": "20271231"}