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NDC 71335-0444-08 Diazepam 10 mg/1 Details

Diazepam 10 mg/1

Diazepam is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is DIAZEPAM.

MedlinePlus Drug Summary

Diazepam is used to relieve anxiety and to control agitation caused by alcohol withdrawal. It is also used along with other medications to control muscle spasms and spasticity caused by certain neurological disorders such as cerebral palsy (condition that causes difficulty with movement and balance), paraplegia (inability to move parts of the body), athetosis (abnormal muscle contractions), and stiff-man syndrome (a rare disorder with muscle rigidity and stiffness). Diazepam is also used along with other medications to control seizures. Diazepam is in a class of medications called benzodiazepines. It works by calming abnormal overactivity in the brain.

Related Packages: 71335-0444-08
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Diazepam

Product Information

NDC	71335-0444
Product ID	71335-0444_fc888abe-fbda-6bda-e053-6294a90af9ed
Associated GPIs	57100040000315
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	Diazepam
Proprietary Name Suffix	n/a
Non-Proprietary Name	Diazepam
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	10
Active Ingredient Units	mg/1
Substance Name	DIAZEPAM
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule	CIV
Marketing Category	ANDA
Application Number	ANDA071322
Listing Certified Through	2024-12-31

Package

NDC 71335-0444-08 (71335044408)

Pricing Information	N/A
NDC Package Code	71335-0444-8
Billing NDC	71335044408
Package	10 TABLET in 1 BOTTLE (71335-0444-8)
Marketing Start Date	2019-03-25
NDC Exclude Flag	N