Package 68071-2213-9

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68071-2213-9
Digits Only 6807122139
Product NDC 68071-2213
Product ID 68071-2213_2abf56a9-a510-5e24-e063-6394a90aa2e7
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-2213-9)

Marketing

Marketing Status
Marketed Since 2020-07-08
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": "2abf56a9-a510-5e24-e063-6394a90aa2e7", "openfda": {"upc": ["0368071221398"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["a9f0e832-e85c-975f-e053-2995a90afa22"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2213-9)", "package_ndc": "68071-2213-9", "marketing_start_date": "20200708"}], "brand_name": "Sildenafil", "product_id": "68071-2213_2abf56a9-a510-5e24-e063-6394a90aa2e7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-2213", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}