NDC 71335-0691 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0691

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075948
Marketed since
September 1, 2002
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
71335-0691-130 TABLET in 1 BOTTLE (71335-0691-1)Feb 15, 2018
71335-0691-260 TABLET in 1 BOTTLE (71335-0691-2)Apr 3, 2024
71335-0691-390 TABLET in 1 BOTTLE (71335-0691-3)Apr 3, 2024
71335-0691-4120 TABLET in 1 BOTTLE (71335-0691-4)Apr 3, 2024
71335-0691-5240 TABLET in 1 BOTTLE (71335-0691-5)Apr 3, 2024
71335-0691-6180 TABLET in 1 BOTTLE (71335-0691-6)Apr 3, 2024
71335-0691-7100 TABLET in 1 BOTTLE (71335-0691-7)Apr 3, 2024

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