Package 68180-283-01

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68180-283-01
Digits Only 6818028301
Product NDC 68180-283
Product ID 68180-283_18727593-f734-4bd5-88eb-625779d35660
Description

1 BOTTLE in 1 CARTON (68180-283-01) / 112 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-09-28
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": "18727593-f734-4bd5-88eb-625779d35660", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["407ee7fc-0022-4fac-9fa6-4285d774fdb3"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68180-283-01)  / 112 mL in 1 BOTTLE", "package_ndc": "68180-283-01", "marketing_start_date": "20220928"}], "brand_name": "SILDENAFIL", "product_id": "68180-283_18727593-f734-4bd5-88eb-625779d35660", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68180-283", "generic_name": "Sildenafil", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA211638", "marketing_category": "ANDA", "marketing_start_date": "20220928", "listing_expiration_date": "20261231"}