NDC 69097-870 – Lanreotide Acetate

Lanreotide Acetate 120 mg/.5mL · Injection · Subcutaneous

Human Prescription Drug 2 recalls

Product NDC69097-870

Product details

Brand name
Lanreotide Acetate
Generic name
lanreotide acetate
Labeler
Cipla USA Inc.
Dosage form
Injection
Route
Subcutaneous
Marketing category
NDA · NDA215395
Marketed since
December 24, 2021
Listing expires
December 31, 2026
Pharmacologic class
Somatostatin Analog

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
69097-870-671 SYRINGE in 1 CARTON (69097-870-67) / .5 mL in 1 SYRINGEDec 24, 2021

Recalls mentioning this NDC

Other Lanreotide Acetate products