FERRIPROX
- Product NDC
- 10122-101
- 11-digit product format
- 101220101
- Labeler code
- 10122
- Product ID
- 10122-101_3ec2a1ae-4ca9-43b3-a3e2-2b79c2a34172
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- deferiprone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Chiesi USA, Inc.
- Application
- NDA208030
- Marketing category
- NDA
- Marketing start
- 2015-09-09
- Substance
- DEFERIPRONE
- Active strength
- 100 mg/mL
- 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
- FERRIPROX
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEFERIPRONE | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2BTY8KH53L |
| Rxcui | 1716264, 1716268 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10122-101-50 | FERRIPROX | 500 mL in 1 BOTTLE, PLASTIC | SOLUTION | 500 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10122-101 | FERRIPROX (DEFERIPRONE) SOLUTION [CHIESI USA, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250525_f057cf4d-b06f-4fbd-aa2e-68c5e4d8a846.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 |
|---|
| 10122-101-50 | 10122010150 | 500 mL in 1 BOTTLE, PLASTIC (10122-101-50) | 500 ml | 2021-01-01 | 0000-00-00 | No | No | Current |