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NDC 65162-0540-50 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 Amneal Pharmaceuticals LLC. 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: 65162-0540-50
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	65162-0540
Product ID	65162-540_cb149fdb-eac2-4e98-9f7a-b06020dfac45
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	Amneal Pharmaceuticals LLC
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078218
Listing Certified Through	2024-12-31

Package

NDC 65162-0540-50 (65162054050)

Pricing Information	N/A
NDC Package Code	65162-540-50
Billing NDC	65162054050
Package	500 TABLET, FILM COATED in 1 BOTTLE (65162-540-50)
Marketing Start Date	2010-02-18
NDC Exclude Flag	N