 
                        | Product NDC: | 55154-5623 | 
| Proprietary Name: | Midodrine HCl | 
| Non Proprietary Name: | midodrine hydrochloride | 
| Active Ingredient(s): | 5 mg/1 & nbsp; midodrine hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 55154-5623 | 
| Labeler Name: | Cardinal Health | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA076725 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20041103 | 
| Package NDC: | 55154-5623-0 | 
| Package Description: | 10 BLISTER PACK in 1 BAG (55154-5623-0) > 1 TABLET in 1 BLISTER PACK | 
| NDC Code | 55154-5623-0 | 
| Proprietary Name | Midodrine HCl | 
| Package Description | 10 BLISTER PACK in 1 BAG (55154-5623-0) > 1 TABLET in 1 BLISTER PACK | 
| Product NDC | 55154-5623 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | midodrine hydrochloride | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20041103 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Cardinal Health | 
| Substance Name | MIDODRINE HYDROCHLORIDE | 
| Strength Number | 5 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |