| NDC Code | 70934-442-60 |
|---|
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-442-60) |
|---|
| Product NDC | 70934-442 |
|---|
| 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 | 20190917 |
|---|
| End Marketing Date | 20241031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208170 |
|---|
| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|