ZA 66 125 mg Pill: blue & white, capsule/oblong, 22mm
The pill with imprint ZA 66 125 mg (Blue & White, Capsule/Oblong, 22mm) has been identified as Divalproex Sodium Delayed-Release (Sprinkle) 125 mg and is used for Bipolar Disorder, Mania, Migraine Prevention, Seizures, and Epilepsy. It belongs to the drug class fatty acid derivative anticonvulsants and is not a controlled substance.
Images for ZA 66 125 mg
Divalproex Sodium Delayed-Release (Sprinkle)
- Imprint
- ZA 66 125 mg
- Strength
- 125 mg
- Color
- Blue & White
- Size
- 22.00 mm
- Shape
- Capsule/Oblong
- Availability
- Prescription only
- Drug Class
- Fatty acid derivative anticonvulsants
- Pregnancy Category
- D - Positive evidence of risk - When treating epilepsy and manic episodes associated with bipolar disorder, X - Not for use in pregnancy - When treating migraine
- CSA Schedule
- Not a controlled drug
- Labeler / Supplier
- Zydus Pharmaceuticals
- Inactive Ingredients
-
alcohol,
ammonia,
butyl alcohol,
microcrystalline cellulose,
FD&C Blue No. 1,
ferrosoferric oxide,
gelatin,
hypromelloses,
isopropyl alcohol,
methacrylic acid,
potassium hydroxide,
propylene glycol,
shellac,
silicon dioxide,
sodium lauryl sulfate,
magnesium silicate,
titanium dioxide,
triethyl citrate,
water
Note: Inactive ingredients may vary.
Labelers / Repackagers
| NDC Code | Labeler / Repackager |
|---|---|
| 68084-0313 | Amerisource Health Services |
| 68382-0106 | Zydus Pharmaceuticals USA Inc. |
See also:
More about divalproex sodium
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Patient resources
Other brands
Depakote, Depakote ER, Depakote Sprinkles
Professional resources
- Divalproex Capsules prescribing information
- Divalproex Delayed Release (FDA)
- Divalproex Delayed Release Tablets (FDA)
- Divalproex Extended Release (FDA)
- Divalproex Sprinkle (FDA)
Other brands
Depakote, Depakote ER, Depakote Sprinkles
Related treatment guides
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.