Mycophenolate Mofetil
- Product NDC
- 17478-422
- 11-digit product format
- 174780422
- Labeler code
- 17478
- Product ID
- 17478-422_266160e8-f5b5-4be3-a2b4-6f5ed8e99b0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate Mofetil
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA204043
- Marketing category
- ANDA
- Marketing start
- 2017-02-28
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 500 mg/20mL
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-422-40 | 17478042240 | 4 VIAL in 1 CARTON (17478-422-40) > 20 mL in 1 VIAL | 4 vial | 2017-02-28 | 0000-00-00 | No | No | Current |