NDC 60760-766 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC60760-766

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine hydrochloride
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
May 31, 2017
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
60760-766-044 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-04)Jun 29, 2023
60760-766-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-15)Jun 29, 2023
60760-766-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-30)May 31, 2017
60760-766-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-90)Nov 1, 2023

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