FERRIPROX
- Product NDC
- 52609-0006
- 11-digit product format
- 526090006
- Labeler code
- 52609
- Product ID
- 52609-0006_e6670b22-0237-7289-57fe-5cc612b842f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- deferiprone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ApoPharma USA, Inc.
- Application
- NDA021825
- Marketing category
- NDA
- Marketing start
- 2011-11-25
- Marketing end
- 0000-00-00
- Substance
- DEFERIPRONE
- Active strength
- 500 mg/1
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52609-0006-1 | FERRIPROX | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 7 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| DEFERIPRONE | ACTIVE INGREDIENT | 2BTY8KH53L | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| DEFERIPRONE | ACTIVE MOIETY | 2BTY8KH53L | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| HYPROMELLOSE 2910 (15000 MPA.S) | INACTIVE INGREDIENT | 288VBX44JC | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| POLYETHYLENE GLYCOL 3350 | INACTIVE INGREDIENT | G2M7P15E5P | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52609-0006 | FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [APOPHARMA USA, INC.] | 7 | Legacy NDC, 1 package rows | 20200305_dc8cbc3d-026c-0db5-42e8-8e93d374dd23.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52609-0006-1 | 52609000601 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52609-0006-1) | 2011-11-25 | 0000-00-00 | No | No | Current |