Valproic Acid
These highlights do not include all the information needed to use VALPROIC ACID CAPSULES safely and effectively. See full prescribing information for VALPROIC ACID CAPSULES.VALPROIC ACID capsules, USP for oral useInitial U.S. Approval: 1978
Approved
Approval ID
8785a152-3010-4370-aaf5-11315a1a56e1
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 30, 2018
Manufacturers
FDA
NCS HealthCare of KY, Inc dba Vangard Labs
DUNS: 050052943
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Valproic Acid
PRODUCT DETAILS
NDC Product Code0615-8205
Application NumberANDA073484
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 30, 2018
Generic NameValproic Acid
INGREDIENTS (7)
VALPROIC ACIDActive
Quantity: 250 mg in 1 1
Code: 614OI1Z5WI
Classification: ACTIB
CORN OILInactive
Code: 8470G57WFM
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT