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Guanfacine Hydrochloride
Guanfacine Hydrochloride - 65162-713-03 - (Guanfacine Hydrochloride)
Drug Information of Guanfacine Hydrochloride
| Product NDC: | 65162-713 |
| Proprietary Name: | Guanfacine Hydrochloride |
| Non Proprietary Name: | Guanfacine Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Guanfacine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guanfacine Hydrochloride
| Product NDC: | 65162-713 |
| Labeler Name: | Amneal Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075109 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981125 |
Package Information of Guanfacine Hydrochloride
| Package NDC: | 65162-713-03 |
| Package Description: | 30 TABLET in 1 BOTTLE (65162-713-03) |
NDC Information of Guanfacine Hydrochloride
| NDC Code | 65162-713-03 |
| Proprietary Name | Guanfacine Hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (65162-713-03) |
| Product NDC | 65162-713 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Guanfacine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19981125 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals |
| Substance Name | GUANFACINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
