| NDC Code | 0615-8084-39 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-39) |
|---|
| Product NDC | 0615-8084 |
|---|
| 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 |
|---|
| End Marketing Date | 20270531 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090478 |
|---|
| Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|