NDC 72888-087 – Oxcarbazepine

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

Human Prescription Drug

Product NDC72888-087

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Advagen Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077747
Marketed since
March 19, 2021
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
72888-087-01100 TABLET, FILM COATED in 1 BOTTLE (72888-087-01)Mar 19, 2021
72888-087-05500 TABLET, FILM COATED in 1 BOTTLE (72888-087-05)Mar 19, 2021
72888-087-3030 TABLET, FILM COATED in 1 BOTTLE (72888-087-30)Mar 19, 2021

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