| NDC Code | 63739-531-10 |
|---|
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-531-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 63739-531 |
|---|
| 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 | 20070228 |
|---|
| End Marketing Date | 20210731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077797 |
|---|
| Manufacturer | McKesson Corporation dba SKY Packaging |
|---|
| Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
|---|