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Methyldopa
Methyldopa - 21695-879-90 - (Methyldopa)
Drug Information of Methyldopa
| Product NDC: | 21695-879 |
| Proprietary Name: | Methyldopa |
| Non Proprietary Name: | Methyldopa |
| Active Ingredient(s): | 250 mg/1 & nbsp; Methyldopa |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methyldopa
| Product NDC: | 21695-879 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070098 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19840220 |
Package Information of Methyldopa
| Package NDC: | 21695-879-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (21695-879-90) |
NDC Information of Methyldopa
| NDC Code | 21695-879-90 |
| Proprietary Name | Methyldopa |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (21695-879-90) |
| Product NDC | 21695-879 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methyldopa |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19840220 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | METHYLDOPA |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
