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DIVALPROEX SODIUM
DIVALPROEX SODIUM - 68084-313-01 - (DIVALPROEX SODIUM)
Drug Information of DIVALPROEX SODIUM
| Product NDC: | 68084-313 |
| Proprietary Name: | DIVALPROEX SODIUM |
| Non Proprietary Name: | DIVALPROEX SODIUM |
| Active Ingredient(s): | 125 mg/1 & nbsp; DIVALPROEX SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED PELLETS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIVALPROEX SODIUM
| Product NDC: | 68084-313 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078919 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090401 |
Package Information of DIVALPROEX SODIUM
| Package NDC: | 68084-313-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-313-01) > 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11) |
NDC Information of DIVALPROEX SODIUM
| NDC Code | 68084-313-01 |
| Proprietary Name | DIVALPROEX SODIUM |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-313-01) > 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68084-313-11) |
| Product NDC | 68084-313 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIVALPROEX SODIUM |
| Dosage Form Name | CAPSULE, COATED PELLETS |
| Route Name | ORAL |
| Start Marketing Date | 20090401 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | DIVALPROEX SODIUM |
| Strength Number | 125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
