NDC 71335-2492 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC71335-2492

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
71335-2492-040 TABLET, FILM COATED in 1 BOTTLE (71335-2492-0)Feb 3, 2025
71335-2492-114 TABLET, FILM COATED in 1 BOTTLE (71335-2492-1)Sep 10, 2024
71335-2492-284 TABLET, FILM COATED in 1 BOTTLE (71335-2492-2)Feb 3, 2025
71335-2492-330 TABLET, FILM COATED in 1 BOTTLE (71335-2492-3)Sep 13, 2024
71335-2492-420 TABLET, FILM COATED in 1 BOTTLE (71335-2492-4)Nov 26, 2024
71335-2492-515 TABLET, FILM COATED in 1 BOTTLE (71335-2492-5)Feb 3, 2025
71335-2492-660 TABLET, FILM COATED in 1 BOTTLE (71335-2492-6)Sep 9, 2024
71335-2492-790 TABLET, FILM COATED in 1 BOTTLE (71335-2492-7)Sep 5, 2024
71335-2492-856 TABLET, FILM COATED in 1 BOTTLE (71335-2492-8)Feb 3, 2025
71335-2492-9120 TABLET, FILM COATED in 1 BOTTLE (71335-2492-9)Oct 4, 2024

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