Package 70518-1844-1

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 70518-1844-1
Digits Only 7051818441
Product NDC 70518-1844
Product ID 70518-1844_4977420c-2205-90c0-e063-6294a90a898d
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)

Marketing

Marketing Status
Marketed Since 2022-12-12
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": "4977420c-2205-90c0-e063-6294a90a898d", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["99bc66a4-05d1-4372-a25a-1153d7af580e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)", "package_ndc": "70518-1844-1", "marketing_start_date": "20221212"}], "brand_name": "Sildenafil", "product_id": "70518-1844_4977420c-2205-90c0-e063-6294a90a898d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70518-1844", "generic_name": "Sildenafil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20190204", "listing_expiration_date": "20271231"}