| NDC Code | 64980-655-10 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (64980-655-10) |
|---|
| Product NDC | 64980-655 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250219 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA218936 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|