NDC 60687-711 – Oxcarbazepine

Oxcarbazepine 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60687-711

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215939
Marketed since
February 2, 2023
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (1)

Package NDCDescriptionSince
60687-711-01100 BLISTER PACK in 1 CARTON (60687-711-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-711-11)Feb 2, 2023

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