Package 68071-3646-1

Brand: sildenafil citrate

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68071-3646-1
Digits Only 6807136461
Product NDC 68071-3646
Product ID 68071-3646_2a2fe9ea-d9e4-9057-e063-6394a90af294
Description

10 TABLET, FILM COATED in 1 BOTTLE (68071-3646-1)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand sildenafil citrate
Generic sildenafil
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": "2a2fe9ea-d9e4-9057-e063-6394a90af294", "openfda": {"upc": ["0368071364613"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["1d614710-708e-f11c-e063-6394a90a05a5"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68071-3646-1)", "package_ndc": "68071-3646-1", "marketing_start_date": "20240716"}], "brand_name": "Sildenafil Citrate", "product_id": "68071-3646_2a2fe9ea-d9e4-9057-e063-6394a90af294", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-3646", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA206401", "marketing_category": "ANDA", "marketing_start_date": "20240716", "listing_expiration_date": "20261231"}