NDCFind

Cyclobenzaprine Hydrochloride 68788-8474

Product NDC

68788-8474
Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
July 1, 2023
Listing Expires
December 31, 2027
Application
ANDA208170
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Active Ingredients

IngredientStrength
Cyclobenzaprine Hydrochloride10 mg/1

Drug Class

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

Packaging Options(5)

20 TABLET, FILM COATED in 1 BOTTLE (68788-8474-2)

30 TABLET, FILM COATED in 1 BOTTLE (68788-8474-3)

15 TABLET, FILM COATED in 1 BOTTLE (68788-8474-5)

60 TABLET, FILM COATED in 1 BOTTLE (68788-8474-6)

90 TABLET, FILM COATED in 1 BOTTLE (68788-8474-9)