| NDC Code | 68258-7150-9 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (68258-7150-9) |
|---|
| Product NDC | 68258-7150 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110829 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078722 |
|---|
| Manufacturer | Dispensing Solutions, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 7.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
|---|