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Dacarbazine
Dacarbazine - 63323-128-20 - (DACARBAZINE)
Drug Information of Dacarbazine
| Product NDC: | 63323-128 |
| Proprietary Name: | Dacarbazine |
| Non Proprietary Name: | DACARBAZINE |
| Active Ingredient(s): | 10 mg/mL & nbsp; DACARBAZINE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dacarbazine
| Product NDC: | 63323-128 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075371 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010907 |
Package Information of Dacarbazine
| Package NDC: | 63323-128-20 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-128-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Dacarbazine
| NDC Code | 63323-128-20 |
| Proprietary Name | Dacarbazine |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-128-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-128 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DACARBAZINE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010907 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | DACARBAZINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
