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"46708-821-10" National Drug Code (NDC)
Divalproex Sodium 100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
(Alembic Pharmaceuticals Limited)
NDC Code
46708-821-10
Package Description
100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC
46708-821
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Divalproex Sodium
Non-Proprietary Name
Divalproex Sodium
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20241223
Marketing Category Name
ANDA
Application Number
ANDA218793
Manufacturer
Alembic Pharmaceuticals Limited
Substance Name
DIVALPROEX SODIUM
Strength
125
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/46708-821-10