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NDC 42806-0565-01 CHLORDIAZEPOXIDE HYDROCHLORIDE 10 mg/1 Details

CHLORDIAZEPOXIDE HYDROCHLORIDE 10 mg/1

CHLORDIAZEPOXIDE HYDROCHLORIDE is a ORAL CAPSULE, GELATIN COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Epic Pharma, LLC. The primary component is CHLORDIAZEPOXIDE HYDROCHLORIDE.

MedlinePlus Drug Summary

Chlordiazepoxide is used to relieve anxiety and to control agitation caused by alcohol withdrawal. Chlordiazepoxide is in a class of medications called benzodiazepines. It works by decreasing abnormal electrical activity in the brain.

Related Packages: 42806-0565-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Chlordiazepoxide

Product Information

NDC	42806-0565
Product ID	42806-565_d7a3306e-01d4-4966-a473-62136d81f959
Associated GPIs	57100020100110
GCN Sequence Number	003734
GCN Sequence Number Description	chlordiazepoxide HCl CAPSULE 10 MG ORAL
HIC3	H20
HIC3 Description	ANTI-ANXIETY - BENZODIAZEPINES
GCN	14031
HICL Sequence Number	001610
HICL Sequence Number Description	CHLORDIAZEPOXIDE HCL
Brand/Generic	Generic
Proprietary Name	CHLORDIAZEPOXIDE HYDROCHLORIDE
Proprietary Name Suffix	n/a
Non-Proprietary Name	CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE, GELATIN COATED
Route	ORAL
Active Ingredient Strength	10
Active Ingredient Units	mg/1
Substance Name	CHLORDIAZEPOXIDE HYDROCHLORIDE
Labeler Name	Epic Pharma, LLC
Pharmaceutical Class	Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule	CIV
Marketing Category	ANDA
Application Number	ANDA085472
Listing Certified Through	2024-12-31

Package

NDC 42806-0565-01 (42806056501)

Pricing Information	N/A
NDC Package Code	42806-565-01
Billing NDC	42806056501
Package	100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-565-01)
Marketing Start Date	2021-08-13
NDC Exclude Flag	N