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NDC 61919-0261-15 CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 Details

CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1

CYCLOBENZAPRINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Direct_Rx. 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: 61919-0261-15
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	61919-0261
Product ID	61919-261_f2126a96-6335-7052-e053-2a95a90af277
Associated GPIs	75100050100304
GCN Sequence Number	062524
GCN Sequence Number Description	cyclobenzaprine HCl TABLET 7.5 MG ORAL
HIC3	H6H
HIC3 Description	SKELETAL MUSCLE RELAXANTS
GCN	98299
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	7.5
Active Ingredient Units	mg/1
Substance Name	CYCLOBENZAPRINE HYDROCHLORIDE
Labeler Name	Direct_Rx
Pharmaceutical Class	Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078722
Listing Certified Through	2024-12-31

Package

NDC 61919-0261-15 (61919026115)

Pricing Information	N/A
NDC Package Code	61919-261-15
Billing NDC	61919026115
Package	15 TABLET, FILM COATED in 1 BOTTLE (61919-261-15)
Marketing Start Date	2019-08-16
NDC Exclude Flag	N