NDC 0641-6030 – Fentanyl Citrate

Fentanyl Citrate 50 ug/mL · Injection · Intravenous

Human Prescription Drug DEA schedule CII 2 recalls

Product NDC0641-6030

Product details

Brand name
Fentanyl Citrate
Generic name
Fentanyl Citrate
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
NDA · NDA019101
Marketed since
July 11, 1984
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fentanyl Citrate →

Package NDC codes (1)

Package NDCDescriptionSince
0641-6030-0150 mL in 1 VIAL (0641-6030-01)Jul 11, 1984

Recalls mentioning this NDC

Other Fentanyl Citrate products