Mycophenolate Mofetil
- Product NDC
- 16714-345
- 11-digit product format
- 167140345
- Labeler code
- 16714
- Product ID
- 16714-345_34a1dff5-eedc-4ab3-903f-0fa5d9fe5a7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate Mofetil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA214525
- Marketing category
- ANDA
- Marketing start
- 2021-07-29
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-345-01 | 16714034501 | 1 BOTTLE, PLASTIC in 1 CARTON (16714-345-01) > 225 mL in 1 BOTTLE, PLASTIC | 2021-07-29 | 0000-00-00 | No | No | Current |