NDC 0093-7334 – Mycophenolate Mofetil

Mycophenolate Mofetil 250 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0093-7334

Product details

Brand name
Mycophenolate Mofetil
Generic name
Mycophenolate Mofetil
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA065491
Marketed since
May 6, 2009
Listing expires
December 31, 2027
Pharmacologic class
Antimetabolite Immunosuppressant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0093-7334-01100 CAPSULE in 1 BOTTLE (0093-7334-01)May 6, 2009
0093-7334-05500 CAPSULE in 1 BOTTLE (0093-7334-05)May 6, 2009

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