Cyclobenzaprine Hydrochloride 70518-3764
Product NDC
70518-3764- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 13, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA078643
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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(2)
12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-0)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3764-1)