Product NDC: | 55045-1167 |
Proprietary Name: | Clonidine Hydrochloride |
Non Proprietary Name: | Clonidine Hydrochloride |
Active Ingredient(s): | .1 mg/1 & nbsp; Clonidine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55045-1167 |
Labeler Name: | Dispensing Solutions, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077901 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070309 |
Package NDC: | 55045-1167-8 |
Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (55045-1167-8) |
NDC Code | 55045-1167-8 |
Proprietary Name | Clonidine Hydrochloride |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (55045-1167-8) |
Product NDC | 55045-1167 |
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 | Dispensing Solutions, Inc. |
Substance Name | CLONIDINE HYDROCHLORIDE |
Strength Number | .1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |