NDC 31722-024 – Oxcarbazepine

Oxcarbazepine 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC31722-024

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215939
Marketed since
January 11, 2022
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
31722-024-01100 TABLET, FILM COATED in 1 BOTTLE (31722-024-01)Jan 11, 2022
31722-024-05500 TABLET, FILM COATED in 1 BOTTLE (31722-024-05)Mar 10, 2023
31722-024-101000 TABLET, FILM COATED in 1 BOTTLE (31722-024-10)Mar 10, 2023
31722-024-3110 BLISTER PACK in 1 CARTON (31722-024-31) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 11, 2022

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