mycophenolate mofetil
- Product NDC
- 50090-2541
- 11-digit product format
- 500902541
- Labeler code
- 50090
- Product ID
- 50090-2541_7bf48260-1219-4f2f-b209-cbb73ca8bdab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolate mofetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065416
- Marketing category
- ANDA
- Marketing start
- 2009-05-04
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2541-0 | 50090254100 | 180 TABLET in 1 BOTTLE (50090-2541-0) | 180 tablet | 2016-10-20 | 0000-00-00 | No | No | Current |