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ProAmatine
ProAmatine - 54092-004-01 - (midodrine hydrochloride)
Drug Information of ProAmatine
| Product NDC: | 54092-004 |
| Proprietary Name: | ProAmatine |
| 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) |
Labeler Information of ProAmatine
| Product NDC: | 54092-004 |
| Labeler Name: | Shire US Manufacturing Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019815 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960906 |
Package Information of ProAmatine
| Package NDC: | 54092-004-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (54092-004-01) |
NDC Information of ProAmatine
| NDC Code | 54092-004-01 |
| Proprietary Name | ProAmatine |
| Package Description | 100 TABLET in 1 BOTTLE (54092-004-01) |
| Product NDC | 54092-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | midodrine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960906 |
| Marketing Category Name | NDA |
| Labeler Name | Shire US Manufacturing Inc. |
| Substance Name | MIDODRINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
