NDC 54288-141 – Mycophenolate Mofetil

Mycophenolate Mofetil Hydrochloride 500 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC54288-141

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil hydrochloride
Labeler
BPI Labs LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA214283
Marketed since
March 8, 2023
Listing expires
December 31, 2027
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

Uses, dosage, side effects and warnings for Mycophenolate Mofetil →

Package NDC codes (1)

Package NDCDescriptionSince
54288-141-044 VIAL in 1 CARTON (54288-141-04) / 20 mL in 1 VIALMar 8, 2023

Other Mycophenolate Mofetil products