NDC Code | 76237-154-30 |
Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-154-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 76237-154 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Divalproex Sodium |
Non-Proprietary Name | Divalproex Sodium |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20111014 |
Marketing Category Name | ANDA |
Application Number | ANDA077567 |
Manufacturer | McKesson Contract Packaging |
Substance Name | DIVALPROEX SODIUM |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |