Package 68788-8153-7

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 68788-8153-7
Digits Only 6878881537
Product NDC 68788-8153
Description

7 TABLET, FILM COATED in 1 BOTTLE (68788-8153-7)

Marketing

Marketing Status
Marketed Since 2022-03-14
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": "4677fe18-0da6-4c0e-989a-d77e4f228a58", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019"], "spl_set_id": ["affacb88-4af3-4ce9-961b-7fc37b169e9a"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (68788-8153-7)", "package_ndc": "68788-8153-7", "marketing_start_date": "20220314"}], "brand_name": "Tadalafil", "product_id": "68788-8153_4677fe18-0da6-4c0e-989a-d77e4f228a58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68788-8153", "generic_name": "Tadalafil", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA209167", "marketing_category": "ANDA", "marketing_start_date": "20220314", "listing_expiration_date": "20271231"}