| NDC Code | 82868-008-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-008-30) |
|---|
| Product NDC | 82868-008 |
|---|
| 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 | 20240429 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078643 |
|---|
| Manufacturer | Northwind Pharmaceuticals, LLC |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
|---|