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Clonidine
Clonidine - 0555-1009-16 - (Clonidine)
Drug Information of Clonidine
| Product NDC: | 0555-1009 |
| Proprietary Name: | Clonidine |
| 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) |
Labeler Information of Clonidine
| Product NDC: | 0555-1009 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079090 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100825 |
Package Information of Clonidine
| Package NDC: | 0555-1009-16 |
| Package Description: | 4 POUCH in 1 CARTON (0555-1009-16) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
NDC Information of Clonidine
| NDC Code | 0555-1009-16 |
| Proprietary Name | Clonidine |
| Package Description | 4 POUCH in 1 CARTON (0555-1009-16) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
| Product NDC | 0555-1009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clonidine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20100825 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | CLONIDINE |
| Strength Number | .1 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
