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Valproate Sodium
Valproate Sodium - 55390-007-10 - (Valproate Sodium)
Drug Information of Valproate Sodium
| Product NDC: | 55390-007 |
| Proprietary Name: | Valproate Sodium |
| Non Proprietary Name: | Valproate Sodium |
| Active Ingredient(s): | 100 mg/mL & nbsp; Valproate Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valproate Sodium
| Product NDC: | 55390-007 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076295 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031206 |
Package Information of Valproate Sodium
| Package NDC: | 55390-007-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (55390-007-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Valproate Sodium
| NDC Code | 55390-007-10 |
| Proprietary Name | Valproate Sodium |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (55390-007-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55390-007 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Valproate Sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20031206 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | VALPROATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
