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Matulane
Matulane - 54482-053-01 - (procarbazine hydrochloride)
Drug Information of Matulane
| Product NDC: | 54482-053 |
| Proprietary Name: | Matulane |
| Non Proprietary Name: | procarbazine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; procarbazine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Matulane
| Product NDC: | 54482-053 |
| Labeler Name: | Sigma-Tau Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016785 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19851227 |
Package Information of Matulane
| Package NDC: | 54482-053-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (54482-053-01) |
NDC Information of Matulane
| NDC Code | 54482-053-01 |
| Proprietary Name | Matulane |
| Package Description | 100 CAPSULE in 1 BOTTLE (54482-053-01) |
| Product NDC | 54482-053 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | procarbazine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19851227 |
| Marketing Category Name | NDA |
| Labeler Name | Sigma-Tau Pharmaceuticals, Inc. |
| Substance Name | PROCARBAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
