Package 72162-2363-9

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 72162-2363-9
Digits Only 7216223639
Product NDC 72162-2363
Product ID 72162-2363_1cf7d6c3-6e03-41e9-a3fd-41ef724ec69c
Description

90 TABLET, FILM COATED in 1 BOTTLE (72162-2363-9)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Sildenafil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cf7d6c3-6e03-41e9-a3fd-41ef724ec69c", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["591a4ae7-e06c-42b6-85af-f03fd2fb8959"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-2363-9)", "package_ndc": "72162-2363-9", "marketing_start_date": "20240716"}], "brand_name": "Sildenafil", "product_id": "72162-2363_1cf7d6c3-6e03-41e9-a3fd-41ef724ec69c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72162-2363", "generic_name": "Sildenafil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203623", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20261231"}