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Guanfacine
Guanfacine - 0591-0453-01 - (Guanfacine)
Drug Information of Guanfacine
| Product NDC: | 0591-0453 |
| Proprietary Name: | Guanfacine |
| Non Proprietary Name: | Guanfacine |
| Active Ingredient(s): | 2 mg/1 & nbsp; Guanfacine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guanfacine
| Product NDC: | 0591-0453 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074145 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951017 |
Package Information of Guanfacine
| Package NDC: | 0591-0453-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0591-0453-01) |
NDC Information of Guanfacine
| NDC Code | 0591-0453-01 |
| Proprietary Name | Guanfacine |
| Package Description | 100 TABLET in 1 BOTTLE (0591-0453-01) |
| Product NDC | 0591-0453 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Guanfacine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19951017 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | GUANFACINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
