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Dantrium
Dantrium - 42023-125-01 - (dantrolene sodium)
Drug Information of Dantrium
| Product NDC: | 42023-125 |
| Proprietary Name: | Dantrium |
| Non Proprietary Name: | dantrolene sodium |
| Active Ingredient(s): | 50 mg/1 & nbsp; dantrolene sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dantrium
| Product NDC: | 42023-125 |
| Labeler Name: | JHP Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017443 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080801 |
Package Information of Dantrium
| Package NDC: | 42023-125-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (42023-125-01) |
NDC Information of Dantrium
| NDC Code | 42023-125-01 |
| Proprietary Name | Dantrium |
| Package Description | 100 CAPSULE in 1 BOTTLE (42023-125-01) |
| Product NDC | 42023-125 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dantrolene sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080801 |
| Marketing Category Name | NDA |
| Labeler Name | JHP Pharmaceuticals LLC |
| Substance Name | DANTROLENE SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC] |
