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NDC 70518-0014-00 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 REMEDYREPACK INC.. 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: 70518-0014-00
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Diazepam

Product Information

NDC	70518-0014
Product ID	70518-0014_0e0cd179-8676-d1a5-e063-6294a90a7ff8
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	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	REMEDYREPACK INC.
Pharmaceutical Class	Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule	CIV
Marketing Category	ANDA
Application Number	ANDA071322
Listing Certified Through	2025-12-31

Package

NDC 70518-0014-00 (70518001400)

Pricing Information	N/A
NDC Package Code	70518-0014-0
Billing NDC	70518001400
Package	30 TABLET in 1 BLISTER PACK (70518-0014-0)
Marketing Start Date	2016-11-30
NDC Exclude Flag	N