DROXIA is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by E.r. Squibb & Sons, L.l.c.. The primary component is Hydroxyurea.
| Product ID | 0003-6337_16f97dab-3e4a-453e-b3b8-f593a15c248e | 
| NDC | 0003-6337 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | DROXIA | 
| Generic Name | Hydroxyurea | 
| Dosage Form | Capsule | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2009-06-01 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA016295 | 
| Labeler Name | E.R. Squibb & Sons, L.L.C. | 
| Substance Name | HYDROXYUREA | 
| Active Ingredient Strength | 400 mg/1 | 
| Pharm Classes | Antimetabolite [EPC],Urea [CS] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2021-12-31 | 
| Marketing Start Date | 2015-07-16 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA016295 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2015-07-16 | 
| Ingredient | Strength | 
|---|---|
| HYDROXYUREA | 400 mg/1 | 
| SPL SET ID: | 740e054b-faac-7c27-f06d-a56efb699355 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0003-6335 | DROXIA | HYDROXYUREA | 
| 0003-6336 | DROXIA | HYDROXYUREA | 
| 0003-6337 | DROXIA | HYDROXYUREA | 
| 0003-0830 | HYDREA | HYDROXYUREA | 
| 0093-0882 | HYDROXYUREA | Hydroxyurea | 
| 0555-0882 | HYDROXYUREA | Hydroxyurea | 
| 0904-6939 | Hydroxyurea | Hydroxyurea | 
| 10135-702 | Hydroxyurea | Hydroxyurea | 
| 24535-0831 | Hydroxyurea | Hydroxyurea | 
| 42291-321 | HYDROXYUREA | Hydroxyurea | 
| 49884-724 | Hydroxyurea | Hydroxyurea | 
| 55154-3554 | Hydroxyurea | Hydroxyurea | 
| 55154-7143 | Hydroxyurea | Hydroxyurea | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  DROXIA  75318230  2222043 Live/Registered | BRISTOL-MYERS SQUIBB COMPANY 1997-07-02 |