Cyclobenzaprine Hydrochloride 76420-0829
Product NDC
76420-0829- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208170
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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(6)
100 TABLET, FILM COATED in 1 BOTTLE (76420-829-01)
7 TABLET, FILM COATED in 1 BOTTLE (76420-829-07)
120 TABLET, FILM COATED in 1 BOTTLE (76420-829-12)
30 TABLET, FILM COATED in 1 BOTTLE (76420-829-30)
60 TABLET, FILM COATED in 1 BOTTLE (76420-829-60)
90 TABLET, FILM COATED in 1 BOTTLE (76420-829-90)