Package 76420-544-30
Brand: tadalafil
Generic: tadalafilPackage Facts
Identity
Package NDC
76420-544-30
Digits Only
7642054430
Product NDC
76420-544
Description
30 TABLET, FILM COATED in 1 BOTTLE (76420-544-30)
Marketing
Marketing Status
Brand
tadalafil
Generic
tadalafil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f7777037-65b9-9411-e053-6294a90a37eb", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "403957", "484814", "757707"], "spl_set_id": ["30ae58ed-5b56-4513-8eb3-eb4f89b78f9d"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-544-30)", "package_ndc": "76420-544-30", "marketing_start_date": "20200219"}], "brand_name": "Tadalafil", "product_id": "76420-544_f7777037-65b9-9411-e053-6294a90a37eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "76420-544", "generic_name": "Tadalafil", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA208934", "marketing_category": "ANDA", "marketing_start_date": "20200219", "listing_expiration_date": "20261231"}