Mycophenolate mofetil
- Product NDC
- 82804-033
- 11-digit product format
- 828040033
- Labeler code
- 82804
- Product ID
- 82804-033_ce06afcb-4e6c-4b78-8bad-9909c8fffa52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate mofetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090456
- Marketing category
- ANDA
- Marketing start
- 2022-10-15
- Substance
- MYCOPHENOLATE MOFETIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Antimetabolite Immunosuppressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9242ECW6R0 | MYCOPHENOLATE MOFETIL | 128794-94-5 | MYCOPHENOLATE MOFETIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-033-30 | 82804003330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-30) | 2023-10-25 | No | No | Historical |
| 82804-033-60 | 82804003360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-60) | 2023-10-25 | No | No | Historical |
| 82804-033-90 | 82804003390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-90) | 2023-10-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mycophenolate mofetil | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |