NDC 71335-2479 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC71335-2479

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
71335-2479-0100 TABLET, FILM COATED in 1 BOTTLE (71335-2479-0)Feb 3, 2025
71335-2479-130 TABLET, FILM COATED in 1 BOTTLE (71335-2479-1)Sep 24, 2024
71335-2479-290 TABLET, FILM COATED in 1 BOTTLE (71335-2479-2)Nov 8, 2024
71335-2479-321 TABLET, FILM COATED in 1 BOTTLE (71335-2479-3)Oct 8, 2024
71335-2479-410 TABLET, FILM COATED in 1 BOTTLE (71335-2479-4)Feb 3, 2025
71335-2479-515 TABLET, FILM COATED in 1 BOTTLE (71335-2479-5)Sep 13, 2024
71335-2479-640 TABLET, FILM COATED in 1 BOTTLE (71335-2479-6)Nov 13, 2024
71335-2479-760 TABLET, FILM COATED in 1 BOTTLE (71335-2479-7)Sep 12, 2024
71335-2479-820 TABLET, FILM COATED in 1 BOTTLE (71335-2479-8)Jan 14, 2025
71335-2479-9120 TABLET, FILM COATED in 1 BOTTLE (71335-2479-9)Sep 12, 2024

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