| NDC Code | 68071-3150-1 |
|---|
| Package Description | 21 TABLET, FILM COATED in 1 BOTTLE (68071-3150-1) |
|---|
| Product NDC | 68071-3150 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160722 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090478 |
|---|
| Manufacturer | NuCare Pharmaceuticals, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|