Package 42291-937-90

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 42291-937-90
Digits Only 4229193790
Product NDC 42291-937
Description

90 TABLET in 1 BOTTLE (42291-937-90)

Marketing

Marketing Status
Marketed Since 2024-09-10
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c0e47e-08b2-0c73-e063-6394a90a90b7", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["21c83ff3-c359-3269-e063-6394a90a57ee"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-937-90)", "package_ndc": "42291-937-90", "marketing_start_date": "20240910"}], "brand_name": "Sildenafil", "product_id": "42291-937_48c0e47e-08b2-0c73-e063-6394a90a90b7", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "42291-937", "generic_name": "Sildenafil", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA202025", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20271231"}