| NDC Code | 60429-052-27 |
|---|
| Package Description | 270 TABLET, FILM COATED in 1 BOTTLE (60429-052-27) |
|---|
| Product NDC | 60429-052 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20120329 |
|---|
| End Marketing Date | 20220930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA071611 |
|---|
| Manufacturer | Golden State Medical Supply, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|