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Hydroxyurea
Hydroxyurea - 49884-724-01 - (Hydroxyurea)
Drug Information of Hydroxyurea
| Product NDC: | 49884-724 |
| 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: | 49884-724 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075340 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990224 |
Package Information of Hydroxyurea
| Package NDC: | 49884-724-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (49884-724-01) |
NDC Information of Hydroxyurea
| NDC Code | 49884-724-01 |
| Proprietary Name | Hydroxyurea |
| Package Description | 100 CAPSULE in 1 BOTTLE (49884-724-01) |
| Product NDC | 49884-724 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyurea |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19990224 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| Substance Name | HYDROXYUREA |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimetabolite [EPC],Urea [Chemical/Ingredient] |
