| NDC Code | 70512-872-10 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10) |
|---|
| Product NDC | 70512-872 |
|---|
| 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 | 20250731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077563 |
|---|
| Manufacturer | SOLA Pharmaceuticals, LLC |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|