Home > National Drug Code (NDC) > DIVALPROEX SODIUM

DIVALPROEX SODIUM - 55648-974-04 - (DIVALPROEX SODIUM)

Alphabetical Index


Drug Information of DIVALPROEX SODIUM

Product NDC: 55648-974
Proprietary Name: DIVALPROEX SODIUM
Non Proprietary Name: DIVALPROEX SODIUM
Active Ingredient(s): 250    mg/1 & nbsp;   DIVALPROEX SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of DIVALPROEX SODIUM

Product NDC: 55648-974
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077296
Marketing Category: ANDA
Start Marketing Date: 20080731

Package Information of DIVALPROEX SODIUM

Package NDC: 55648-974-04
Package Description: 100 BLISTER PACK in 1 CARTON (55648-974-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of DIVALPROEX SODIUM

NDC Code 55648-974-04
Proprietary Name DIVALPROEX SODIUM
Package Description 100 BLISTER PACK in 1 CARTON (55648-974-04) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55648-974
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIVALPROEX SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080731
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
Substance Name DIVALPROEX SODIUM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of DIVALPROEX SODIUM


General Information