NDC 66689-307 – Mycophenolate Mofetil

Mycophenolate Mofetil 200 mg/mL · Powder, For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC66689-307

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
VistaPharm, LLC
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA210370
Marketed since
February 15, 2019
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
66689-307-081 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTICFeb 15, 2019

Recalls mentioning this NDC

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