Cyclobenzaprine Hcl 85509-1001
Product NDC
85509-1001- Manufacturer
- Phoenix Rx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 25, 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(4)
120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1)
30 TABLET, FILM COATED in 1 BOTTLE (85509-1001-3)
60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6)
90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9)