NDC 0480-9262 – Octreotide Acetate

· Kit · Intramuscular

Human Prescription Drug 4 recalls

Product NDC0480-9262

Product details

Brand name
Octreotide Acetate
Generic name
Octreotide Acetate
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Kit
Route
Intramuscular
Marketing category
ANDA · ANDA210317
Marketed since
October 1, 2024
Listing expires
December 31, 2026

Active ingredients

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

    Package NDC codes (1)

    Package NDCDescriptionSince
    0480-9262-081 KIT in 1 KIT (0480-9262-08) * 8 mL in 1 VIAL, SINGLE-DOSE (0480-9260-01) * 2 mL in 1 SYRINGE (0480-9263-21)Oct 1, 2024

    Recalls mentioning this NDC

    Other Octreotide Acetate products