Mycophenolic Acid
- Product NDC
- 50268-559
- 11-digit product format
- 502680559
- Labeler code
- 50268
- Product ID
- 50268-559_ed85a3b9-991f-a59c-e053-2a95a90abcb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolic Acid
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA091558
- Marketing category
- ANDA
- Marketing start
- 2021-01-27
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE SODIUM
- Active strength
- 180 mg/1
- 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 |
|---|
| 50268-559-12 | 50268055912 | 20 BLISTER PACK in 1 BOX (50268-559-12) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-559-11) | 20 blister pack | 2021-01-27 | 0000-00-00 | No | No | Current |