Mycophenolic Acid
- Product NDC
- 72322-1048
- 11-digit product format
- 723221048
- Labeler code
- 72322
- Product ID
- 72322-1048_bbab286d-00d9-9e22-e053-2995a90a5a9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolic Acid
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AMTA LABS LIMITED
- Application
- ANDA214376
- Marketing category
- ANDA
- Marketing start
- 2021-12-31
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72322-1048-1 | 72322104801 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (72322-1048-1) | 2021-12-31 | 0000-00-00 | No | No | Current |
| 72322-1048-2 | 72322104802 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72322-1048-2) | 2021-12-31 | 0000-00-00 | No | No | Current |