NDC 67457-239 – Octreotide Acetate

Octreotide Acetate 50 ug/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug 1 recall

Product NDC67457-239

Product details

Brand name
Octreotide Acetate
Generic name
Octreotide acetate
Labeler
Mylan Institutional LLC
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA079198
Marketed since
April 1, 2011
Listing expires
December 31, 2026
Pharmacologic class
Somatostatin Analog

Active ingredients

Uses, dosage, side effects and warnings for Octreotide Acetate →

Package NDC codes (1)

Package NDCDescriptionSince
67457-239-0110 SYRINGE in 1 CARTON (67457-239-01) / 1 mL in 1 SYRINGE (67457-239-00)Apr 1, 2011

Recalls mentioning this NDC

Other Octreotide Acetate products