Mycophenolate Mofetil
- Product NDC
- 0480-1175
- 11-digit product format
- 004801175
- Labeler code
- 0480
- Product ID
- 0480-1175_eb033330-c721-4af7-ba51-6cd79bc24aa4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate Mofetil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA211272
- Marketing category
- ANDA
- Marketing start
- 2022-06-02
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 200 mg/mL
- 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 |
|---|
| 0480-1175-22 | 00480117522 | 1 BOTTLE in 1 CARTON (0480-1175-22) > 225 mL in 1 BOTTLE | 1 bottle | 2022-06-02 | 0000-00-00 | No | No | Current |