NDC 70518-4692 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4692

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA218936
Marketed since
July 7, 2026
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-4692-030 TABLET in 1 BOTTLE, PLASTIC (70518-4692-0)Jul 7, 2026
70518-4692-112 TABLET in 1 BOTTLE, PLASTIC (70518-4692-1)Sep 2, 2026

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