Package 82009-093-01

Brand: sildenafil citrate

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 82009-093-01
Digits Only 8200909301
Product NDC 82009-093
Description

100 TABLET, FILM COATED in 1 BOTTLE (82009-093-01)

Marketing

Marketing Status
Marketed Since 2023-07-19
Brand sildenafil citrate
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "853230e4-4f33-420e-bd3c-d5b45f4e0689", "openfda": {"upc": ["0382009093017"], "unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["41b67fd2-3d9a-49d6-88b8-285044b98dc1"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (82009-093-01)", "package_ndc": "82009-093-01", "marketing_start_date": "20230719"}], "brand_name": "Sildenafil Citrate", "product_id": "82009-093_853230e4-4f33-420e-bd3c-d5b45f4e0689", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82009-093", "generic_name": "Sildenafil", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA206401", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}