NDC 71335-2110 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2110

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078643
Marketed since
September 26, 2008
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
71335-2110-040 TABLET, FILM COATED in 1 BOTTLE (71335-2110-0)Jun 20, 2022
71335-2110-114 TABLET, FILM COATED in 1 BOTTLE (71335-2110-1)Jun 20, 2022
71335-2110-284 TABLET, FILM COATED in 1 BOTTLE (71335-2110-2)Jun 20, 2022
71335-2110-330 TABLET, FILM COATED in 1 BOTTLE (71335-2110-3)Jun 20, 2022
71335-2110-420 TABLET, FILM COATED in 1 BOTTLE (71335-2110-4)Jun 20, 2022
71335-2110-515 TABLET, FILM COATED in 1 BOTTLE (71335-2110-5)Jun 20, 2022
71335-2110-660 TABLET, FILM COATED in 1 BOTTLE (71335-2110-6)Jun 20, 2022
71335-2110-790 TABLET, FILM COATED in 1 BOTTLE (71335-2110-7)Jun 20, 2022
71335-2110-856 TABLET, FILM COATED in 1 BOTTLE (71335-2110-8)Jun 20, 2022
71335-2110-9120 TABLET, FILM COATED in 1 BOTTLE (71335-2110-9)Jun 20, 2022

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