Package 65862-688-90
Brand: sildenafil
Generic: sildenafilPackage Facts
Identity
Package NDC
65862-688-90
Digits Only
6586268890
Product NDC
65862-688
Description
90 TABLET, FILM COATED in 1 BOTTLE (65862-688-90)
Marketing
Marketing Status
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": "aee36818-4865-49b7-9f54-29c62f8d4fda", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["17621e92-79a0-46aa-86c7-ea179e81928d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-688-90)", "package_ndc": "65862-688-90", "marketing_start_date": "20151118"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-688-99)", "package_ndc": "65862-688-99", "marketing_start_date": "20151118"}], "brand_name": "Sildenafil", "product_id": "65862-688_aee36818-4865-49b7-9f54-29c62f8d4fda", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "65862-688", "generic_name": "Sildenafil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203963", "marketing_category": "ANDA", "marketing_start_date": "20151118", "listing_expiration_date": "20271231"}