NDC 71335-2666 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2666

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA218936
Marketed since
February 19, 2025
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
71335-2666-040 TABLET in 1 BOTTLE (71335-2666-0)Jul 14, 2025
71335-2666-114 TABLET in 1 BOTTLE (71335-2666-1)Jul 14, 2025
71335-2666-284 TABLET in 1 BOTTLE (71335-2666-2)Jul 14, 2025
71335-2666-330 TABLET in 1 BOTTLE (71335-2666-3)Jul 14, 2025
71335-2666-420 TABLET in 1 BOTTLE (71335-2666-4)Jul 14, 2025
71335-2666-515 TABLET in 1 BOTTLE (71335-2666-5)Jul 14, 2025
71335-2666-660 TABLET in 1 BOTTLE (71335-2666-6)Jul 14, 2025
71335-2666-790 TABLET in 1 BOTTLE (71335-2666-7)Jul 14, 2025
71335-2666-856 TABLET in 1 BOTTLE (71335-2666-8)Jul 14, 2025
71335-2666-9120 TABLET in 1 BOTTLE (71335-2666-9)Jul 14, 2025

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