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NDC 68788-9967-06 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 Preferred Pharmaceuticals, Inc.. 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: 68788-9967-06
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Cyclobenzaprine

Product Information

NDC	68788-9967
Product ID	68788-9967_34b5f2c8-deda-41f0-baf8-8761aebf1ed6
Associated GPIs	75100050100304
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	7.5
Active Ingredient Units	mg/1
Substance Name	CYCLOBENZAPRINE HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
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 68788-9967-06 (68788996706)

Pricing Information	N/A
NDC Package Code	68788-9967-6
Billing NDC	68788996706
Package	60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6)
Marketing Start Date	2015-05-01
NDC Exclude Flag	N