Mycophenolate Mofetil
- Product NDC
- 70748-262
- 11-digit product format
- 707480262
- Labeler code
- 70748
- Product ID
- 70748-262_ecc0d5bc-feca-4534-80c3-331e0fe63b28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolate mofetil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA212087
- Marketing category
- ANDA
- Marketing start
- 2020-12-21
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 500 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70748-262-01 | 70748026201 | 100 TABLET in 1 BOTTLE (70748-262-01) | 100 tablet | 2020-12-21 | 0000-00-00 | No | No | Current |
| 70748-262-02 | 70748026202 | 500 TABLET in 1 BOTTLE (70748-262-02) | 500 tablet | 2020-12-21 | 0000-00-00 | No | No | Current |