NDCFind

Cyclobenzaprine Hydrochloride 68071-2659-05

Package NDC

68071-2659-05

Product NDC: 68071-2659

Manufacturer
Nucare Pharmaceuticals,inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
September 26, 2008
Listing Expires
December 31, 2026
Application
ANDA078643
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Active Ingredients

IngredientStrength
Cyclobenzaprine Hydrochloride10 mg/1

Drug Class

Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]

Selected Package

68071-2659-05Selected

15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)

Other packages for this product(3)

30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)

6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)

14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)