Package 71821-009-01

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 71821-009-01
Digits Only 7182100901
Product NDC 71821-009
Product ID 71821-009_d0fb5849-3fc9-11d3-e053-2995a90a5bbc
Description

30 TABLET, FILM COATED in 1 BOTTLE (71821-009-01)

Marketing

Marketing Status
Marketed Since 2021-11-04
Brand tadalafil
Generic tadalafil
Sample Package No

Linked Drug Pages (1)

tadalafil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d0fb5849-3fc9-11d3-e053-2995a90a5bbc", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0371821009016", "0371821006015", "0371821007029", "0371821007012"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "403957", "484814", "757707"], "spl_set_id": ["b4d9851c-5c06-4532-bd82-16d92b60c28f"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["VKT Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71821-009-01)", "package_ndc": "71821-009-01", "marketing_start_date": "20211104"}], "brand_name": "tadalafil", "product_id": "71821-009_d0fb5849-3fc9-11d3-e053-2995a90a5bbc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71821-009", "generic_name": "Tadalafil", "labeler_name": "VKT Pharma Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA215556", "marketing_category": "ANDA", "marketing_start_date": "20211104", "listing_expiration_date": "20261231"}