MYLAN 2250 MYLAN 2250 Pill - tan purple capsule/oblong, 19mm
Pill with imprint MYLAN 2250 MYLAN 2250 is Tan / Purple, Capsule/Oblong and has been identified as Mycophenolate Mofetil 250 mg. It is supplied by Mylan Pharmaceuticals Inc.
Mycophenolate mofetil is used in the treatment of Nephrotic Syndrome; Organ Transplant, Rejection Prophylaxis; Graft-versus-host disease and belongs to the drug class selective immunosuppressants. There is positive evidence of human fetal risk during pregnancy. Mycophenolate mofetil 250 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for MYLAN 2250 MYLAN 2250
Mycophenolate Mofetil
- Imprint
- MYLAN 2250 MYLAN 2250
- Strength
- 250 mg
- Color
- Tan / Purple
- Size
- 19.00 mm
- Shape
- Capsule/Oblong
- Availability
- Prescription only
- Drug Class
- Selective immunosuppressants
- Pregnancy Category
- D - Positive evidence of risk
- CSA Schedule
- Not a controlled drug
- Labeler / Supplier
- Mylan Pharmaceuticals Inc.
- Inactive Ingredients
-
silicon dioxide,
croscarmellose sodium,
magnesium stearate,
microcrystalline cellulose,
corn starch,
sodium lauryl sulfate,
ferrosoferric oxide,
FD&C Blue No. 2,
gelatin,
ferric oxide red,
titanium dioxide,
ferric oxide yellow,
ammonia,
propylene glycol,
shellac
Note: Inactive ingredients may vary.
Labelers / Repackagers
| NDC Code | Labeler / Repackager |
|---|---|
| 00378-2250 | Mylan Pharmaceuticals Inc. |
| 51079-0721 | UDL Laboratories Inc. |
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Patient resources
- Mycophenolate mofetil oral/injection drug information
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Professional resources
- Mycophenolate monograph
- Mycophenolate (FDA)
- Mycophenolate Mofetil (FDA)
- Mycophenolate Mofetil Injection (FDA)
- Mycophenolate Suspension (FDA)
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Further information
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