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Lomustine
Lomustine - 58181-3030-5 - (lomustine)
Drug Information of Lomustine
| Product NDC: | 58181-3030 |
| Proprietary Name: | Lomustine |
| Non Proprietary Name: | lomustine |
| Active Ingredient(s): | 10 mg/1 & nbsp; lomustine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lomustine
| Product NDC: | 58181-3030 |
| Labeler Name: | NextSource Biotechnology, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Start Marketing Date: | 20130523 |
Package Information of Lomustine
| Package NDC: | 58181-3030-5 |
| Package Description: | 5 CAPSULE, GELATIN COATED in 1 BOTTLE (58181-3030-5) |
NDC Information of Lomustine
| NDC Code | 58181-3030-5 |
| Proprietary Name | Lomustine |
| Package Description | 5 CAPSULE, GELATIN COATED in 1 BOTTLE (58181-3030-5) |
| Product NDC | 58181-3030 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lomustine |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130523 |
| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Labeler Name | NextSource Biotechnology, LLC |
| Substance Name | LOMUSTINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
