Mycophenolic Acid
- Product NDC
- 0093-7032
- 11-digit product format
- 000937032
- Labeler code
- 0093
- Product ID
- 0093-7032_bf343b58-06a3-4598-b95b-980c85b2970a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolic Acid
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA202720
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- Marketing end
- 2021-05-31
- Substance
- MYCOPHENOLATE SODIUM
- Active strength
- 360 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7032-89 | 00093703289 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-7032-89) | 2019-08-15 | 2021-05-31 | No | No | Current |