NDCFind

Cyclobenzaprine Hydrochloride 71335-2110-01

Package NDC

71335-2110-01

Product NDC: 71335-2110

Manufacturer
Bryant Ranch Prepack
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

71335-2110-01Selected

14 TABLET, FILM COATED in 1 BOTTLE (71335-2110-1)

Other packages for this product(9)

40 TABLET, FILM COATED in 1 BOTTLE (71335-2110-0)

84 TABLET, FILM COATED in 1 BOTTLE (71335-2110-2)

30 TABLET, FILM COATED in 1 BOTTLE (71335-2110-3)

20 TABLET, FILM COATED in 1 BOTTLE (71335-2110-4)

15 TABLET, FILM COATED in 1 BOTTLE (71335-2110-5)

60 TABLET, FILM COATED in 1 BOTTLE (71335-2110-6)

90 TABLET, FILM COATED in 1 BOTTLE (71335-2110-7)

56 TABLET, FILM COATED in 1 BOTTLE (71335-2110-8)

120 TABLET, FILM COATED in 1 BOTTLE (71335-2110-9)