DEFERIPRONE
- Product NDC
- 75907-349
- 11-digit product format
- 759070349
- Labeler code
- 75907
- Product ID
- 75907-349_c3247274-c72a-4181-9638-58f7ff14729c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- deferiprone
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- DR. REDDY'S LABORATORIES, INC.
- Application
- ANDA220132
- Marketing category
- ANDA
- Marketing start
- 2025-12-15
- 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 |
|---|
| 75907-349-01 | DEFERIPRONE | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 75907-349-01 | 75907034901 | 100 TABLET, COATED in 1 BOTTLE (75907-349-01) | 2025-12-15 | No | No | Current |