NDC 71335-2514 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 15 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2514

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091281
Marketed since
March 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
71335-2514-130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2514-1)Oct 24, 2024
71335-2514-290 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2514-2)Oct 24, 2024
71335-2514-360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2514-3)Oct 24, 2024

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