Product NDC: | 21695-567 |
Proprietary Name: | Catapres |
Non Proprietary Name: | clonidine |
Active Ingredient(s): | .1 mg/24h & nbsp; clonidine |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-567 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018891 |
Marketing Category: | NDA |
Start Marketing Date: | 19851001 |
Package NDC: | 21695-567-04 |
Package Description: | 4 POUCH in 1 CARTON (21695-567-04) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
NDC Code | 21695-567-04 |
Proprietary Name | Catapres |
Package Description | 4 POUCH in 1 CARTON (21695-567-04) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
Product NDC | 21695-567 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clonidine |
Dosage Form Name | PATCH, EXTENDED RELEASE |
Route Name | TRANSDERMAL |
Start Marketing Date | 19851001 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CLONIDINE |
Strength Number | .1 |
Strength Unit | mg/24h |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |