Deferasirox
- Product NDC
- 72205-389
- 11-digit product format
- 722050389
- Labeler code
- 72205
- Product ID
- 72205-389_a03c7657-fdca-4acb-ad82-c24680e90eae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Deferasirox
- Dosage form
- TABLET, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Novadoz Pharmaceuticals LLC
- Application
- ANDA209878
- Marketing category
- ANDA
- Marketing start
- 2019-11-20
- Substance
- DEFERASIROX
- Active strength
- 125 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Iron Chelating Activity [MoA], Iron Chelator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Deferasirox
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEFERASIROX | 125 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V8G4MOF2V9 |
| Rxcui | 597768, 597770, 597772 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72205-389-01 | Deferasirox | 30 in 1 BOTTLE | TABLET, FOR SUSPENSION | 30 | | 1 |
| 72205-389-02 | Deferasirox | 90 in 1 BOTTLE | TABLET, FOR SUSPENSION | 90 | | 1 |
| 72205-389-03 | Deferasirox | 1000 in 1 BOTTLE | TABLET, FOR SUSPENSION | 1000 | | 1 |
| 72205-389-05 | Deferasirox | 10 in 1 CARTON | TABLET, FOR SUSPENSION | 10 | | 1 |
| 72205-389-05 | Deferasirox | 10 in 1 BLISTER PACK | TABLET, FOR SUSPENSION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72205-389-01 | 72205038901 | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-389-01) | | 2026-01-29 | No | No | Current |
| 72205-389-02 | 72205038902 | 90 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-389-02) | | 2026-01-29 | No | No | Current |
| 72205-389-03 | 72205038903 | 1000 TABLET, FOR SUSPENSION in 1 BOTTLE (72205-389-03) | | 2026-01-29 | No | No | Current |
| 72205-389-05 | 72205038905 | 10 BLISTER PACK in 1 CARTON (72205-389-05) / 10 TABLET, FOR SUSPENSION in 1 BLISTER PACK | 10 blister pack | 2026-01-29 | No | No | Current |