Cyclobenzaprine Hydrochloride 69420-1001
Product NDC
69420-1001- Manufacturer
- Sa3, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 2015
- Listing Expires
- December 31, 2026
- 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(3)
1000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)
100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)
30 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)