Mycophenolate Mofetil
- Product NDC
- 55154-5382
- 11-digit product format
- 551545382
- Labeler code
- 55154
- Product ID
- 55154-5382_700941b9-de3e-49c7-bca2-f85663cdf223
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolate mofetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA065521
- Marketing category
- ANDA
- Marketing start
- 2011-10-25
- Marketing end
- 2030-01-31
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 55154-5382-0 | 55154538200 | 10 BLISTER PACK in 1 BAG (55154-5382-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2011-10-25 | 0000-00-00 | No | No | Current |