Home
>
National Drug Code (NDC)
>
Clonidine Hydrochloride
Clonidine Hydrochloride - 50436-3524-3 - (clonidine hydrochloride)
Drug Information of Clonidine Hydrochloride
| Product NDC: | 50436-3524 |
| Proprietary Name: | Clonidine Hydrochloride |
| Non Proprietary Name: | clonidine hydrochloride |
| Active Ingredient(s): | .2 mg/1 & nbsp; clonidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clonidine Hydrochloride
| Product NDC: | 50436-3524 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077901 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070309 |
Package Information of Clonidine Hydrochloride
| Package NDC: | 50436-3524-3 |
| Package Description: | 90 TABLET in 1 BOTTLE (50436-3524-3) |
NDC Information of Clonidine Hydrochloride
| NDC Code | 50436-3524-3 |
| Proprietary Name | Clonidine Hydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE (50436-3524-3) |
| Product NDC | 50436-3524 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clonidine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070309 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | CLONIDINE HYDROCHLORIDE |
| Strength Number | .2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
