Package 53746-351-90
Brand: sildenafil
Generic: sildenafilPackage Facts
Identity
Package NDC
53746-351-90
Digits Only
5374635190
Product NDC
53746-351
Description
90 TABLET in 1 BOTTLE (53746-351-90)
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": "7548032b-9e89-4c6e-996c-f5ccc07a74d4", "openfda": {"upc": ["0353746351906"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["a0b734f4-9347-484d-b307-d493ae50ee54"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (53746-351-90)", "package_ndc": "53746-351-90", "marketing_start_date": "20121108"}], "brand_name": "Sildenafil", "product_id": "53746-351_7548032b-9e89-4c6e-996c-f5ccc07a74d4", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "53746-351", "generic_name": "Sildenafil", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA202025", "marketing_category": "ANDA", "marketing_start_date": "20121108", "listing_expiration_date": "20261231"}