NDC 70771-1842 – Oxcarbazepine

Oxcarbazepine 150 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1842

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Zydus Lifesciences Limited
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 (3)

Package NDCDescriptionSince
70771-1842-1100 TABLET in 1 BOTTLE (70771-1842-1)Jul 10, 2025
70771-1842-410 BLISTER PACK in 1 CARTON (70771-1842-4) / 10 TABLET in 1 BLISTER PACKJul 10, 2025
70771-1842-5500 TABLET in 1 BOTTLE (70771-1842-5)Jul 10, 2025

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