NDC 85509-1014 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC85509-1014

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
PHOENIX RX LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
March 20, 2025
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
85509-1014-330 TABLET, FILM COATED in 1 BOTTLE (85509-1014-3)Jul 22, 2025
85509-1014-660 TABLET, FILM COATED in 1 BOTTLE (85509-1014-6)Jul 22, 2025
85509-1014-990 TABLET, FILM COATED in 1 BOTTLE (85509-1014-9)Jul 22, 2025

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