mycophenolic acid
- Product NDC
- 70748-217
- 11-digit product format
- 707480217
- Labeler code
- 70748
- Product ID
- 70748-217_9ee6d1b6-60ce-459c-b8bf-dcc3a4158f63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolic acid
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA211173
- Marketing category
- ANDA
- Marketing start
- 2020-04-03
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70748-217-16 | 70748021716 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (70748-217-16) | 2020-04-03 | 0000-00-00 | No | No | Current |