Package 47335-012-83

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 47335-012-83
Digits Only 4733501283
Product NDC 47335-012
Product ID 47335-012_5f176ab2-0dba-4418-8aee-27a110ed6396
Description

30 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)

Marketing

Marketing Status
Marketed Since 2019-03-26
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": "5f176ab2-0dba-4418-8aee-27a110ed6396", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0347335010831", "0347335012835", "0347335011838"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "403957", "484814", "757707"], "spl_set_id": ["168a135b-1454-4def-9b03-c9a470bfcb5f"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)", "package_ndc": "47335-012-83", "marketing_start_date": "20190326"}], "brand_name": "Tadalafil", "product_id": "47335-012_5f176ab2-0dba-4418-8aee-27a110ed6396", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "47335-012", "generic_name": "Tadalafil", "labeler_name": "Sun Pharmaceutical Industries, 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": "20190326", "listing_expiration_date": "20261231"}