MYCOPHENOLATE MOFETIL
- Product NDC
- 72603-751
- 11-digit product format
- 726030751
- Labeler code
- 72603
- Product ID
- 72603-751_127eabe2-8386-452a-ad6b-d879e1f2c099
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mycophenolate mofetil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA218227
- Marketing category
- ANDA
- Marketing start
- 2026-03-01
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MYCOPHENOLATE MOFETIL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MYCOPHENOLATE MOFETIL | 200 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9242ECW6R0 |
| Rxcui | 311880 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-751-01 | MYCOPHENOLATE MOFETIL | 1 in 1 CARTON | POWDER, FOR SUSPENSION | 1 | | 1 |
| 72603-751-01 | MYCOPHENOLATE MOFETIL | 225 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 225 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-751-01 | 72603075101 | 1 BOTTLE in 1 CARTON (72603-751-01) / 225 mL in 1 BOTTLE | 1 bottle | 2026-03-01 | No | No | Historical |