NDC Code(s) : 61786-104-02
Packager : REMEDYREPACK INC.
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : none
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
| Divalproex SodiumDivalproex Sodium TABLET, DELAYED RELEASE | ||||||||||||||||||||||||||||||||||||||||||||||||||
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PRINCIPAL DISPLAY PANEL
DRUG: Divalproex Sodium
GENERIC: Divalproex Sodium
DOSAGE: TABLET, DELAYED RELEASE
ADMINSTRATION: ORAL
NDC: 61786-104-02
COLOR: pink
SHAPE: OVAL
SCORE: No score
SIZE: 14 mm
IMPRINT: UL;250
PACKAGING: 30 in 1 BLISTER PACK
ACTIVE INGREDIENT(S):
- DIVALPROEX SODIUM 250mg in 1
INACTIVE INGREDIENT(S):
- ALCOHOL
- SODIUM BICARBONATE
- SILICON DIOXIDE
- SHELLAC
- SODIUM LAURYL SULFATE
- PROPYLENE GLYCOL
- STARCH, PREGELATINIZED CORN
- TRIETHYL CITRATE
- TALC
- TITANIUM DIOXIDE
- TRIACETIN
- POLYETHYLENE GLYCOL 3000
- CELLULOSE, MICROCRYSTALLINE
- D&C RED NO. 30
- FD&C BLUE NO. 2
- BUTYL ALCOHOL
- FERRIC OXIDE RED
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- FERROSOFERRIC OXIDE
- LACTOSE MONOHYDRATE
- ISOPROPYL ALCOHOL
- HYPROMELLOSE 2910 (6 MPA.S)
- VANILLIN
