NDC 71335-2696 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 30 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2696

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021777
Marketed since
March 4, 2019
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
71335-2696-130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-1)Sep 24, 2025
71335-2696-260 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2696-2)Sep 24, 2025

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