Search by Drug Name or NDC

NDC 50436-9805-01 Cyclobenzaprine Hydrochloride 5 mg/1 Details

Cyclobenzaprine Hydrochloride 5 mg/1

Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by UNIT DOSE SERVICES. 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: 50436-9805-01
Last Updated: 04/14/2024
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	50436-9805
Product ID	50436-9805_ec14f35b-29dd-4c21-916a-88e366e7a7d1
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	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	5
Active Ingredient Units	mg/1
Substance Name	CYCLOBENZAPRINE HYDROCHLORIDE
Labeler Name	UNIT DOSE SERVICES
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078643
Listing Certified Through	2024-12-31

Package

NDC 50436-9805-01 (50436980501)

Pricing Information	N/A
NDC Package Code	50436-9805-1
Billing NDC	50436980501
Package	30 TABLET, FILM COATED in 1 BOTTLE (50436-9805-1)
Marketing Start Date	2023-07-11
NDC Exclude Flag	N