Deferiprone
- Product NDC
- 51672-4237
- 11-digit product format
- 516724237
- Labeler code
- 51672
- Product ID
- 51672-4237_3631d351-4653-3512-e063-6394a90a81c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Deferiprone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA208800
- Marketing category
- ANDA
- Marketing start
- 2024-02-05
- Substance
- DEFERIPRONE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Iron Chelating Activity [MoA], Iron Chelator [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 |
|---|
| 2BTY8KH53L | DEFERIPRONE | 30652-11-0 | DEFERIPRONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51672-4237-4 | 51672423704 | 50 TABLET in 1 BOTTLE (51672-4237-4) | 50 tablet | 2024-02-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Deferiprone | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries, Ltd. | 2025-05-28 | HUMAN PRESCRIPTION DRUG LABEL | 16 |