Cyclobenzaprine Hydrochloride 68788-8221
Product NDC
68788-8221- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 9, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA078643
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyclobenzaprine Hydrochloride | 5 mg/1 |
Drug Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(5)
20 TABLET, FILM COATED in 1 BOTTLE (68788-8221-2)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8221-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-8221-6)
120 TABLET, FILM COATED in 1 BOTTLE (68788-8221-8)
90 TABLET, FILM COATED in 1 BOTTLE (68788-8221-9)