Cyclobenzaprine Hydrochloride 70518-3814
Product NDC
70518-3814- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 1, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA208170
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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(4)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-0)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-2)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-3)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-5)