Product Detail
- National Drug Code
- 60505-2965
- 11 Digit NDC Code
- 60505-2965-9
- Type
- HUMAN PRESCRIPTION DRUG
- Proprietary Name
- Mycophenolic Acid
- Proprietary Name Suffix
- Non-Proprietary Name
- Mycophenolic Acid
- Package Description
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-9)
- Dosage Form
- TABLET, DELAYED RELEASE
- Route of Administration
- ORAL
- Start Marketing
- 8/21/2012
- End Marketing
- 6/30/2021
- Marketing Category
- ANDA
- Application Number
- ANDA091558
- Labeler
- Apotex Corp
- Active Ingredients
-
- MYCOPHENOLATE SODIUM 180mg/1
- Pharmacological Classes
- Antimetabolite Immunosuppressant [EPC]
- DEA Schedule
Additional Packages
Clicking on the package will display details
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-1)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-3)
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-5)
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-6)
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-7)
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-8)
NDC Database last updated 12/18/2020
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