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Dantrolene Sodium
Dantrolene Sodium - 68084-300-21 - (Dantrolene Sodium)
Drug Information of Dantrolene Sodium
| Product NDC: | 68084-300 |
| Proprietary Name: | Dantrolene Sodium |
| Non Proprietary Name: | Dantrolene Sodium |
| Active Ingredient(s): | 25 mg/1 & nbsp; Dantrolene Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dantrolene Sodium
| Product NDC: | 68084-300 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076856 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080925 |
Package Information of Dantrolene Sodium
| Package NDC: | 68084-300-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-300-21) > 10 CAPSULE in 1 BLISTER PACK (68084-300-11) |
NDC Information of Dantrolene Sodium
| NDC Code | 68084-300-21 |
| Proprietary Name | Dantrolene Sodium |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-300-21) > 10 CAPSULE in 1 BLISTER PACK (68084-300-11) |
| Product NDC | 68084-300 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dantrolene Sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080925 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | DANTROLENE SODIUM |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC] |
