Valproic (Page 12 of 12)

PRINCIPAL DISPLAY PANEL


NDC 17856-4012 -01

Valproic Acid
Capsules, USP
250 mg
100 CapsulesRx Only

image 1
(click image for full-size original)
image 2

VALPROIC valproic acid capsule, liquid filled
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:17856-4012(NDC:0591-4012)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VALPROIC ACID (VALPROIC ACID) VALPROIC ACID 250 mg
Inactive Ingredients
Ingredient Name Strength
PEANUT OIL
GLYCERIN
GELATIN
TITANIUM DIOXIDE
Product Characteristics
Color WHITE (off-white) Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code VALPROIC;250
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:17856-4012-1 100 POUCH in 1 BOX, UNIT-DOSE contains a POUCH
1 1 CAPSULE, LIQUID FILLED in 1 POUCH This package is contained within the BOX, UNIT-DOSE (17856-4012-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA073229 09/08/2009
Labeler — ATLANTIC BIOLOGICALS CORP. (047437707)
Establishment
Name Address ID/FEI Operations
ATLANTIC BIOLOGICALS CORP. 047437707 relabel (17856-4012), repack (17856-4012)

Revised: 08/2020 ATLANTIC BIOLOGICALS CORP.

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2024. All Rights Reserved.