| NDC Code | 24979-035-04 |
|---|
| Package Description | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-035-04) |
|---|
| Product NDC | 24979-035 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190301 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091281 |
|---|
| Manufacturer | TWi Pharmaceuticals, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|