NDC 0641-6175 – Octreotide Acetate

Octreotide Acetate 100 ug/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug

Product NDC0641-6175

Product details

Brand name
Octreotide Acetate
Generic name
Octreotide Acetate
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA076313
Marketed since
April 4, 2005
Listing expires
December 31, 2027
Pharmacologic class
Somatostatin Analog

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0641-6175-1010 VIAL, SINGLE-DOSE in 1 CARTON (0641-6175-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6175-01)Apr 4, 2005

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