Deferiprone
- Product NDC
- 51672-4196
- 11-digit product format
- 516724196
- Labeler code
- 51672
- Product ID
- 51672-4196_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
- 500 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Deferiprone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEFERIPRONE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2BTY8KH53L |
| Rxcui | 389242, 2180997 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51672-4196-1 | Deferiprone | 100 in 1 BOTTLE | TABLET | 100 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-4196 | DEFERIPRONE TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 15 | Current NDC, Legacy NDC, 1 package rows | 20250523_5af1643d-4c6e-4668-ae9b-1046f0ad6d8a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51672-4196-1 | 51672419601 | 100 TABLET in 1 BOTTLE (51672-4196-1) | 100 tablet | 2024-02-05 | 0000-00-00 | No | No | Current |