mycophenolate mofetil
- Product NDC
- 70518-2835
- 11-digit product format
- 705182835
- Labeler code
- 70518
- Product ID
- 70518-2835_d7703da8-7905-369e-e053-2a95a90aa485
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolate mofetil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090253
- Marketing category
- ANDA
- Marketing start
- 2020-08-18
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2835 | MYCOPHENOLATE MOFETIL CAPSULE [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250403_90336570-e701-4f50-a19f-b5e7d6f2d293.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2835-0 | 70518283500 | 100 POUCH in 1 BOX (70518-2835-0) > 1 CAPSULE in 1 POUCH (70518-2835-1) | 100 pouch | 2020-08-18 | 0000-00-00 | No | No | Current |