Product NDC: | 55154-5093 |
Proprietary Name: | Methyldopa |
Non Proprietary Name: | methyldopa |
Active Ingredient(s): | 250 mg/1 & nbsp; methyldopa |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-5093 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070076 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110823 |
Package NDC: | 55154-5093-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-5093-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-5093-0 |
Proprietary Name | Methyldopa |
Package Description | 10 BLISTER PACK in 1 BAG (55154-5093-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-5093 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | methyldopa |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110823 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | METHYLDOPA |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |