Product NDC: | 54092-515 |
Proprietary Name: | Intuniv |
Non Proprietary Name: | guanfacine |
Active Ingredient(s): | 2 mg/1 & nbsp; guanfacine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54092-515 |
Labeler Name: | Shire US Manufacturing Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022037 |
Marketing Category: | NDA |
Start Marketing Date: | 20090902 |
Package NDC: | 54092-515-02 |
Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (54092-515-02) |
NDC Code | 54092-515-02 |
Proprietary Name | Intuniv |
Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (54092-515-02) |
Product NDC | 54092-515 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | guanfacine |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20090902 |
Marketing Category Name | NDA |
Labeler Name | Shire US Manufacturing Inc. |
Substance Name | GUANFACINE HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |