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"68788-7183-3" National Drug Code (NDC)
Divalproex Sodium 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-3)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7183-3
Package Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-7183-3)
Product NDC
68788-7183
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20180717
Marketing Category Name
ANDA
Application Number
ANDA079163
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
DIVALPROEX SODIUM
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7183-3