NDC 71205-678 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC71205-678

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-678-3030 TABLET, FILM COATED in 1 BOTTLE (71205-678-30)Jul 27, 2022
71205-678-6060 TABLET, FILM COATED in 1 BOTTLE (71205-678-60)Jul 27, 2022
71205-678-9090 TABLET, FILM COATED in 1 BOTTLE (71205-678-90)Jul 27, 2022

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