NDC 51655-818 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-818

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
January 31, 2023
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
51655-818-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-26)Jan 31, 2023
51655-818-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-52)Feb 28, 2023
51655-818-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-818-53)Aug 24, 2023

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