FERRIPROX
- Product NDC
- 52609-4502
- 11-digit product format
- 526094502
- Labeler code
- 52609
- Product ID
- 52609-4502_8e4e4a6d-8849-1baf-77ee-90e536bb6b84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- deferiprone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ApoPharma USA, Inc.
- Application
- NDA208030
- Marketing category
- NDA
- Marketing start
- 2015-09-09
- Marketing end
- 0000-00-00
- Substance
- DEFERIPRONE
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Iron Chelating Activity [MoA],Iron Chelator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52609-4502-7 | 52609450207 | 500 mL in 1 BOTTLE, PLASTIC (52609-4502-7) | 500 ml | 2015-09-09 | 0000-00-00 | No | No | Current |