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Divalproex Sodium
Divalproex Sodium - 63739-554-10 - (Divalproex Sodium)
Drug Information of Divalproex Sodium
| Product NDC: | 63739-554 |
| Proprietary Name: | Divalproex Sodium |
| Non Proprietary Name: | Divalproex Sodium |
| Active Ingredient(s): | 500 mg/1 & nbsp; Divalproex Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Divalproex Sodium
| Product NDC: | 63739-554 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078853 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120123 |
Package Information of Divalproex Sodium
| Package NDC: | 63739-554-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-554-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Divalproex Sodium
| NDC Code | 63739-554-10 |
| Proprietary Name | Divalproex Sodium |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-554-10) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 63739-554 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Divalproex Sodium |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120123 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | DIVALPROEX SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
