NDC 51655-427 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC51655-427

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
September 1, 2020
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
51655-427-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-26)Apr 1, 2021
51655-427-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-52)Apr 13, 2022
51655-427-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-53)Sep 1, 2020

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