AN 757 Pill: white, capsule/oblong, 21mm
The pill with imprint AN 757 (White, Capsule/Oblong, 21mm) has been identified as Divalproex Sodium Extended-Release 500 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 AN 757
Divalproex Sodium Extended-Release
- Imprint
- AN 757
- Strength
- 500 mg
- Color
- White
- Size
- 21.00 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
- Amneal Pharmaceuticals
- National Drug Code (NDC)
- 65162-0757
- Inactive Ingredients
-
ammonia,
methacrylic acid - methyl methacrylate copolymer (1:1),
hypromelloses,
ferrosoferric oxide,
isopropyl alcohol,
lactose monohydrate,
polyethylene glycol,
magnesium stearate,
microcrystalline cellulose,
butyl alcohol,
propylene glycol,
shellac,
silicon dioxide,
magnesium silicate,
titanium dioxide
Note: Inactive ingredients may vary.
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.