NDC 68071-2659 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC68071-2659

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078643
Marketed since
September 26, 2008
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68071-2659-330 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)Mar 28, 2022
68071-2659-515 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)Mar 28, 2022
68071-2659-66 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)Oct 14, 2024
68071-2659-714 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)Dec 2, 2024

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