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NDC 71335-1089-04 CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 Details

CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1

CYCLOBENZAPRINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Cyclobenzaprine is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Cyclobenzaprine is in a class of medications called skeletal muscle relaxants. It works by acting in the brain and nervous system to allow the muscles to relax.

Related Packages: 71335-1089-04
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	71335-1089
Product ID	71335-1089_fb51afd9-e542-4a23-9f67-f8a0e417a986
Associated GPIs	75100050100305
GCN Sequence Number	004681
GCN Sequence Number Description	cyclobenzaprine HCl TABLET 10 MG ORAL
HIC3	H6H
HIC3 Description	SKELETAL MUSCLE RELAXANTS
GCN	18020
HICL Sequence Number	001950
HICL Sequence Number Description	CYCLOBENZAPRINE HCL
Brand/Generic	Generic
Proprietary Name	CYCLOBENZAPRINE HYDROCHLORIDE
Proprietary Name Suffix	n/a
Non-Proprietary Name	CYCLOBENZAPRINE HYDROCHLORIDE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	10
Active Ingredient Units	mg/1
Substance Name	CYCLOBENZAPRINE HYDROCHLORIDE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078218
Listing Certified Through	2023-12-31

Package

NDC 71335-1089-04 (71335108904)

Pricing Information	N/A
NDC Package Code	71335-1089-4
Billing NDC	71335108904
Package	20 TABLET, FILM COATED in 1 BOTTLE (71335-1089-4)
Marketing Start Date	2019-02-22
NDC Exclude Flag	N