NDC 70748-274 – Ganirelix Acetate

Ganirelix Acetate 250 ug/.5mL · Injection, Solution · Subcutaneous

Human Prescription Drug 1 recall

Product NDC70748-274

Product details

Brand name
Ganirelix Acetate
Generic name
Ganirelix Acetate
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
ANDA · ANDA216075
Marketed since
February 14, 2024
Listing expires
December 31, 2026
Pharmacologic class
Gonadotropin Releasing Hormone Receptor Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70748-274-011 TRAY in 1 CARTON (70748-274-01) / 1 SYRINGE, GLASS in 1 TRAY / 1 mL in 1 SYRINGE, GLASSFeb 14, 2024

Recalls mentioning this NDC

Other Ganirelix Acetate products