NDC 51655-973 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC51655-973

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090478
Marketed since
May 4, 2022
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
51655-973-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-20)Oct 17, 2022
51655-973-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-25)Sep 6, 2022
51655-973-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-52)Oct 7, 2022
51655-973-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-53)Jul 27, 2022
51655-973-5415 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)Aug 24, 2022
51655-973-876 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87)May 4, 2022

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