Mycophenolate Mofetil
- Product NDC
- 60687-427
- 11-digit product format
- 606870427
- Labeler code
- 60687
- Product ID
- 60687-427_b101efba-c8db-6251-e053-2995a90ae223
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate Mofetil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA090055
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- Marketing end
- 0000-00-00
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 60687-427-01 | 60687042701 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-427-01) > 1 CAPSULE in 1 BLISTER PACK (60687-427-11) | 100 blister pack | 2020-10-01 | 0000-00-00 | No | No | Current |