NDC 71335-0461 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0461

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074649
Marketed since
October 3, 1996
Listing expires
December 31, 2026
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Carbamazepine →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0461-130 TABLET in 1 BOTTLE (71335-0461-1)Jul 13, 2020
71335-0461-260 TABLET in 1 BOTTLE (71335-0461-2)May 29, 2024
71335-0461-390 TABLET in 1 BOTTLE (71335-0461-3)May 29, 2024
71335-0461-4120 TABLET in 1 BOTTLE (71335-0461-4)May 29, 2024
71335-0461-5240 TABLET in 1 BOTTLE (71335-0461-5)May 29, 2024
71335-0461-6180 TABLET in 1 BOTTLE (71335-0461-6)May 29, 2024
71335-0461-7100 TABLET in 1 BOTTLE (71335-0461-7)Sep 16, 2025

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