DEFERASIROX
- Product NDC
- 62332-411
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEFERASIROX
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Inc.
- Application
- ANDA211824
- Marketing category
- ANDA
- Substance
- DEFERASIROX
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 62332-411-30 | 30 TABLET, FILM COATED in 1 BOTTLE (62332-411-30) | 2020-06-15 | | No | Historical |
| 62332-411-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (62332-411-91) | 2020-06-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DEFERASIROX | Alembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited | 2023-02-28 | Human Prescription Drug Label | 17 |