| NDC Code | 0615-8508-05 |
|---|
| Package Description | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8508-05) |
|---|
| Product NDC | 0615-8508 |
|---|
| 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 | 20200706 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213324 |
|---|
| Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|