NDC 59746-720 – Eslicarbazepine Acetate

Eslicarbazepine Acetate 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59746-720

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
59746-720-05500 TABLET in 1 BOTTLE (59746-720-05)May 1, 2026
59746-720-3030 TABLET in 1 BOTTLE (59746-720-30)May 1, 2026
59746-720-9090 TABLET in 1 BOTTLE (59746-720-90)May 1, 2026

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