| Product NDC: | 54868-0533 |
| Proprietary Name: | Catapres |
| Non Proprietary Name: | clonidine |
| Active Ingredient(s): | .3 mg/1 & nbsp; clonidine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-0533 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018891 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040708 |
| Package NDC: | 54868-0533-0 |
| Package Description: | 4 POUCH in 1 CARTON (54868-0533-0) > 1 PATCH, EXTENDED RELEASE in 1 POUCH |
| NDC Code | 54868-0533-0 |
| Proprietary Name | Catapres |
| Package Description | 4 POUCH in 1 CARTON (54868-0533-0) > 1 PATCH, EXTENDED RELEASE in 1 POUCH |
| Product NDC | 54868-0533 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clonidine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20040708 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CLONIDINE |
| Strength Number | .3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |