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Mustargen
Mustargen - 67386-911-51 - (mechlorethamine hydrochloride)
Drug Information of Mustargen
| Product NDC: | 67386-911 |
| Proprietary Name: | Mustargen |
| Non Proprietary Name: | mechlorethamine hydrochloride |
| Active Ingredient(s): | 10 mg/10mL & nbsp; mechlorethamine hydrochloride |
| Administration Route(s): | INTRACAVITARY; INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mustargen
| Product NDC: | 67386-911 |
| Labeler Name: | Lundbeck LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA006695 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19490315 |
Package Information of Mustargen
| Package NDC: | 67386-911-51 |
| Package Description: | 4 VIAL, SINGLE-DOSE in 1 BOX (67386-911-51) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Mustargen
| NDC Code | 67386-911-51 |
| Proprietary Name | Mustargen |
| Package Description | 4 VIAL, SINGLE-DOSE in 1 BOX (67386-911-51) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 67386-911 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mechlorethamine hydrochloride |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRACAVITARY; INTRAVENOUS |
| Start Marketing Date | 19490315 |
| Marketing Category Name | NDA |
| Labeler Name | Lundbeck LLC |
| Substance Name | MECHLORETHAMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
