| NDC Code | 0378-1065-93 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-1065-93) |
|---|
| Product NDC | 0378-1065 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Guanfacine Hydrochloride |
|---|
| Non-Proprietary Name | Guanfacine |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150602 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202578 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | GUANFACINE HYDROCHLORIDE |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
|---|