Cyclobenzaprine Hydrochloride 68788-9967
Product NDC
68788-9967- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA078722
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyclobenzaprine Hydrochloride | 7.5 mg/1 |
Drug Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(7)
100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1)
20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2)
30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6)
8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7)
120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8)
90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9)