Package 82009-094-90

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 82009-094-90
Digits Only 8200909490
Product NDC 82009-094
Product ID 82009-094_3548d614-f7d1-4628-88b8-c5cae1178df0
Description

90 TABLET in 1 BOTTLE (82009-094-90)

Marketing

Marketing Status
Marketed Since 2023-07-19
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": "3548d614-f7d1-4628-88b8-c5cae1178df0", "openfda": {"upc": ["0382009094908"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["333ca682-931f-4edb-95d6-2edbd87631cf"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82009-094-90)", "package_ndc": "82009-094-90", "marketing_start_date": "20230719"}], "brand_name": "Sildenafil", "product_id": "82009-094_3548d614-f7d1-4628-88b8-c5cae1178df0", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82009-094", "generic_name": "Sildenafil", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA210394", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}