Package 68071-3832-3

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68071-3832-3
Digits Only 6807138323
Product NDC 68071-3832
Product ID 68071-3832_3314cf58-b7ab-c69f-e063-6294a90aab33
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3832-3)

Marketing

Marketing Status
Marketed Since 2025-04-18
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": "3314cf58-b7ab-c69f-e063-6294a90aab33", "openfda": {"upc": ["0368071383232"], "unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["3314d14e-99eb-39e5-e063-6394a90aed94"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3832-3)", "package_ndc": "68071-3832-3", "marketing_start_date": "20250418"}], "brand_name": "Sildenafil", "product_id": "68071-3832_3314cf58-b7ab-c69f-e063-6294a90aab33", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-3832", "generic_name": "Sildenafil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA203962", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}