NDC 0641-6029 – Fentanyl Citrate

Fentanyl Citrate 50 ug/mL · Injection · Intravenous

Human Prescription Drug DEA schedule CII 2 recalls

Product NDC0641-6029

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 (2)

Package NDCDescriptionSince
0641-6029-0120 mL in 1 VIAL (0641-6029-01)Jul 11, 1984
0641-6029-2525 VIAL in 1 CARTON (0641-6029-25) / 20 mL in 1 VIAL (0641-6029-01)Jul 11, 1984

Recalls mentioning this NDC

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