Package 68071-3908-1

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 68071-3908-1
Digits Only 6807139081
Product NDC 68071-3908
Description

10 TABLET, FILM COATED in 1 BOTTLE (68071-3908-1)

Marketing

Marketing Status
Marketed Since 2025-10-21
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": "41b2c18b-9ec3-4dae-e063-6294a90a8923", "openfda": {"upc": ["0368071390810"], "unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["41b2c017-53a0-c687-e063-6394a90a15b2"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68071-3908-1)", "package_ndc": "68071-3908-1", "marketing_start_date": "20251021"}], "brand_name": "Sildenafil", "product_id": "68071-3908_41b2c18b-9ec3-4dae-e063-6294a90a8923", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68071-3908", "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"}