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TENEX
TENEX - 67857-705-01 - (guanfacine hydrochloride)
Drug Information of TENEX
| Product NDC: | 67857-705 |
| Proprietary Name: | TENEX |
| 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) |
Labeler Information of TENEX
| Product NDC: | 67857-705 |
| Labeler Name: | Promius Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019032 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19861027 |
Package Information of TENEX
| Package NDC: | 67857-705-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (67857-705-01) |
NDC Information of TENEX
| NDC Code | 67857-705-01 |
| Proprietary Name | TENEX |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (67857-705-01) |
| Product NDC | 67857-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | guanfacine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19861027 |
| Marketing Category Name | NDA |
| Labeler Name | Promius Pharma, LLC |
| Substance Name | GUANFACINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
