NDC 71335-0096 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0096

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078722
Marketed since
March 25, 2015
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0096-010 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0)Mar 9, 2022
71335-0096-160 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1)Mar 20, 2018
71335-0096-230 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2)Mar 5, 2018
71335-0096-390 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3)Mar 20, 2018
71335-0096-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4)May 9, 2018
71335-0096-515 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5)Sep 27, 2019
71335-0096-645 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6)Mar 9, 2022
71335-0096-79 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7)Sep 4, 2018
71335-0096-8180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8)Mar 9, 2022
71335-0096-914 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9)Apr 23, 2018

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