Home
>
National Drug Code (NDC)
>
HYDROXYUREA
HYDROXYUREA - 0555-0882-02 - (Hydroxyurea)
Drug Information of HYDROXYUREA
| Product NDC: | 0555-0882 |
| Proprietary Name: | HYDROXYUREA |
| Non Proprietary Name: | Hydroxyurea |
| Active Ingredient(s): | 500 mg/1 & nbsp; Hydroxyurea |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYDROXYUREA
| Product NDC: | 0555-0882 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075143 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981019 |
Package Information of HYDROXYUREA
| Package NDC: | 0555-0882-02 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0555-0882-02) |
NDC Information of HYDROXYUREA
| NDC Code | 0555-0882-02 |
| Proprietary Name | HYDROXYUREA |
| Package Description | 100 CAPSULE in 1 BOTTLE (0555-0882-02) |
| Product NDC | 0555-0882 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyurea |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19981019 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | HYDROXYUREA |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimetabolite [EPC],Urea [Chemical/Ingredient] |
