Cyclobenzaprine Hydrochloride 70518-4692
Product NDC
70518-4692- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 7, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA218936
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyclobenzaprine Hydrochloride | 10 mg/1 |
Drug Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
30 TABLET in 1 BOTTLE, PLASTIC (70518-4692-0)