NDC 71335-1099 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1099

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
May 31, 2017
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
71335-1099-0100 TABLET, FILM COATED in 1 BOTTLE (71335-1099-0)Feb 22, 2019
71335-1099-130 TABLET, FILM COATED in 1 BOTTLE (71335-1099-1)Feb 22, 2019
71335-1099-290 TABLET, FILM COATED in 1 BOTTLE (71335-1099-2)Feb 22, 2019
71335-1099-321 TABLET, FILM COATED in 1 BOTTLE (71335-1099-3)Feb 22, 2019
71335-1099-410 TABLET, FILM COATED in 1 BOTTLE (71335-1099-4)Feb 22, 2019
71335-1099-515 TABLET, FILM COATED in 1 BOTTLE (71335-1099-5)Feb 22, 2019
71335-1099-640 TABLET, FILM COATED in 1 BOTTLE (71335-1099-6)Feb 22, 2019
71335-1099-760 TABLET, FILM COATED in 1 BOTTLE (71335-1099-7)Feb 22, 2019
71335-1099-820 TABLET, FILM COATED in 1 BOTTLE (71335-1099-8)Feb 22, 2019
71335-1099-9120 TABLET, FILM COATED in 1 BOTTLE (71335-1099-9)Feb 22, 2019

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