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NDC 70518-2254-00 OXCARBAZEPINE 600 mg/1 Details

OXCARBAZEPINE 600 mg/1

OXCARBAZEPINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is OXCARBAZEPINE.

MedlinePlus Drug Summary

Oxcarbazepine (Trileptal) is used alone or in combination with other medications to control certain types of seizures in adults and children. Oxcarbazepine extended-release tablets (Oxtellar XR) are used in combination with other medications to control certain types of seizures in adults and children 6 years of age and older. Oxcarbazepine is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.

Related Packages: 70518-2254-00
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Oxcarbazepine

Product Information

NDC	70518-2254
Product ID	70518-2254_0b37bfd0-426b-16e7-e063-6394a90aeb68
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	OXCARBAZEPINE
Proprietary Name Suffix	n/a
Non-Proprietary Name	OXCARBAZEPINE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	600
Active Ingredient Units	mg/1
Substance Name	OXCARBAZEPINE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical Class	Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078069
Listing Certified Through	2024-12-31

Package

NDC 70518-2254-00 (70518225400)

Pricing Information	N/A
NDC Package Code	70518-2254-0
Billing NDC	70518225400
Package	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2254-0)
Marketing Start Date	2019-08-05
NDC Exclude Flag	N