NDC 71288-568 – Octreotide Acetate

Octreotide Acetate 500 ug/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug

Product NDC71288-568

Product details

Brand name
Octreotide Acetate
Generic name
Octreotide Acetate
Labeler
Meitheal Pharmaceuticals, Inc.
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA075957
Marketed since
February 28, 2025
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
71288-568-0210 VIAL, SINGLE-DOSE in 1 CARTON (71288-568-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-568-01)Feb 28, 2025

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