Product NDC: | 67457-218 |
Proprietary Name: | Duraclon |
Non Proprietary Name: | clonidine hydrochloride |
Active Ingredient(s): | .1 mg/mL & nbsp; clonidine hydrochloride |
Administration Route(s): | EPIDURAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67457-218 |
Labeler Name: | Mylan Institutional LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020615 |
Marketing Category: | NDA |
Start Marketing Date: | 19961002 |
Package NDC: | 67457-218-10 |
Package Description: | 1 VIAL in 1 CARTON (67457-218-10) > 10 mL in 1 VIAL |
NDC Code | 67457-218-10 |
Proprietary Name | Duraclon |
Package Description | 1 VIAL in 1 CARTON (67457-218-10) > 10 mL in 1 VIAL |
Product NDC | 67457-218 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clonidine hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | EPIDURAL |
Start Marketing Date | 19961002 |
Marketing Category Name | NDA |
Labeler Name | Mylan Institutional LLC |
Substance Name | CLONIDINE HYDROCHLORIDE |
Strength Number | .1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |