Cyclobenzaprine Hydrochloride 70518-4265
Product NDC
70518-4265- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 24, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA213324
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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(1)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4265-0)