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NDC 61919-0901-30 CYCLOBENZAPRINE HCL 5 mg/1 Details

CYCLOBENZAPRINE HCL 5 mg/1

CYCLOBENZAPRINE HCL is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECTRX. 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: 61919-0901-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	61919-0901
Product ID	61919-901_fd766c38-e406-49e5-e053-6294a90aaf36
Associated GPIs	75100050100303
GCN Sequence Number	047478
GCN Sequence Number Description	cyclobenzaprine HCl TABLET 5 MG ORAL
HIC3	H6H
HIC3 Description	SKELETAL MUSCLE RELAXANTS
GCN	12805
HICL Sequence Number	001950
HICL Sequence Number Description	CYCLOBENZAPRINE HCL
Brand/Generic	Generic
Proprietary Name	CYCLOBENZAPRINE HCL
Proprietary Name Suffix	n/a
Non-Proprietary Name	CYCLOBENZAPRINE HCL
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	CYCLOBENZAPRINE HYDROCHLORIDE
Labeler Name	DIRECTRX
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077797
Listing Certified Through	2024-12-31

Package

NDC 61919-0901-30 (61919090130)

Pricing Information	N/A
NDC Package Code	61919-901-30
Billing NDC	61919090130
Package	30 TABLET, FILM COATED in 1 BOTTLE (61919-901-30)
Marketing Start Date	2019-04-04
NDC Exclude Flag	N