NDC 59746-717 – Eslicarbazepine Acetate

Eslicarbazepine Acetate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59746-717

Product details

Brand name
Eslicarbazepine Acetate
Generic name
eslicarbazepine acetate
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211219
Marketed since
May 1, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Eslicarbazepine acetate →

Package NDC codes (3)

Package NDCDescriptionSince
59746-717-101000 TABLET in 1 BOTTLE (59746-717-10)May 1, 2026
59746-717-3030 TABLET in 1 BOTTLE (59746-717-30)May 1, 2026
59746-717-9090 TABLET in 1 BOTTLE (59746-717-90)May 1, 2026

Other Eslicarbazepine acetate products