NDC 68071-3462 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC68071-3462

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
cyclobenzaprine hydrochloride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208170
Marketed since
May 31, 2017
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
68071-3462-220 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2)Jul 19, 2023
68071-3462-330 TABLET, FILM COATED in 1 BOTTLE (68071-3462-3)Jul 31, 2023
68071-3462-515 TABLET, FILM COATED in 1 BOTTLE (68071-3462-5)Jul 19, 2023

Other Cyclobenzaprine Hydrochloride products