| Product NDC: | 55154-6218 |
| Proprietary Name: | Guanfacine |
| Non Proprietary Name: | Guanfacine Hydrochloride |
| Active Ingredient(s): | 1 mg/1 & nbsp; Guanfacine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-6218 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074796 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970127 |
| Package NDC: | 55154-6218-4 |
| Package Description: | 100 POUCH in 1 CARTON (55154-6218-4) > 1 TABLET in 1 POUCH (55154-6218-6) |
| NDC Code | 55154-6218-4 |
| Proprietary Name | Guanfacine |
| Package Description | 100 POUCH in 1 CARTON (55154-6218-4) > 1 TABLET in 1 POUCH (55154-6218-6) |
| Product NDC | 55154-6218 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Guanfacine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970127 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | GUANFACINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |