Package 31722-776-31

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 31722-776-31
Digits Only 3172277631
Product NDC 31722-776
Description

10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-31)

Marketing

Marketing Status
Marketed Since 2014-11-26
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15e66fb9-9c64-563b-e063-6394a90a5194", "openfda": {"upc": ["0331722776905"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["f9415142-a5ac-45c0-a7c2-fb1fb6751f3d"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-776-05)", "package_ndc": "31722-776-05", "marketing_start_date": "20141126"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-31)", "package_ndc": "31722-776-31", "marketing_start_date": "20141126"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-32)", "package_ndc": "31722-776-32", "marketing_start_date": "20141126"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-33)", "package_ndc": "31722-776-33", "marketing_start_date": "20141126"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-34)", "package_ndc": "31722-776-34", "marketing_start_date": "20141126"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-776-90)", "package_ndc": "31722-776-90", "marketing_start_date": "20141126"}], "brand_name": "Sildenafil", "product_id": "31722-776_15e66fb9-9c64-563b-e063-6394a90a5194", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "31722-776", "generic_name": "Sildenafil", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203623", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20261231"}