NDC 68382-692 – Oxcarbazepine

Oxcarbazepine 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-692

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211747
Marketed since
July 10, 2025
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (4)

Package NDCDescriptionSince
68382-692-01100 TABLET in 1 BOTTLE (68382-692-01)Jul 10, 2025
68382-692-05500 TABLET in 1 BOTTLE (68382-692-05)Jul 10, 2025
68382-692-101000 TABLET in 1 BOTTLE (68382-692-10)Jul 10, 2025
68382-692-3010 BLISTER PACK in 1 CARTON (68382-692-30) / 10 TABLET in 1 BLISTER PACKJul 10, 2025

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