| NDC Code | 68387-500-60 |
|---|
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (68387-500-60) |
|---|
| Product NDC | 68387-500 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060824 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA071611 |
|---|
| Manufacturer | Keltman Pharmaceuticals Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
|---|