NDC 68083-515 – Octreotide Acetate

Octreotide Acetate 200 ug/mL · Injection, Solution · Intravenous, Subcutaneous

Human Prescription Drug

Product NDC68083-515

Product details

Brand name
Octreotide Acetate
Generic name
Octreotide Acetate
Labeler
Gland Pharma Limited
Dosage form
Injection, Solution
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA216807
Marketed since
June 13, 2023
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
68083-515-011 VIAL in 1 CARTON (68083-515-01) / 5 mL in 1 VIALJun 13, 2023

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