Package 0641-6290-01

Brand: fentanyl citrate

Generic: fentanyl citrate
NDC Package

Package Facts

Identity

Package NDC 0641-6290-01
Digits Only 0641629001
Product NDC 0641-6290
Description

1 VIAL in 1 CARTON (0641-6290-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-08-29
Brand fentanyl citrate
Generic fentanyl citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "133a8135-0c15-44cc-86c1-5acb6819fc1a", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["1735003", "1735008"], "spl_set_id": ["c5fcdcbd-1dd1-4ebf-aa0d-edfe845414b7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0641-6290-01)  / 20 mL in 1 VIAL", "package_ndc": "0641-6290-01", "marketing_start_date": "20250829"}], "brand_name": "Fentanyl Citrate", "product_id": "0641-6290_133a8135-0c15-44cc-86c1-5acb6819fc1a", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6290", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "50 ug/mL"}], "application_number": "NDA019101", "marketing_category": "NDA", "marketing_start_date": "20250829", "listing_expiration_date": "20271231"}