Package 68071-4674-3

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68071-4674-3
Digits Only 6807146743
Product NDC 68071-4674
Product ID 68071-4674_1ab89447-6691-2646-e063-6394a90a3679
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4674-3)

Marketing

Marketing Status
Marketed Since 2018-12-19
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": "1ab89447-6691-2646-e063-6394a90a3679", "openfda": {"upc": ["0368071467437"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["7d68a3d3-590b-0bd9-e053-2a91aa0ae8cd"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4674-3)", "package_ndc": "68071-4674-3", "marketing_start_date": "20181219"}], "brand_name": "Sildenafil", "product_id": "68071-4674_1ab89447-6691-2646-e063-6394a90a3679", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-4674", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}