| NDC Code | 53002-3081-2 |
|---|
| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (53002-3081-2) |
|---|
| Product NDC | 53002-3081 |
|---|
| 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 | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|