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Methyldopa
Methyldopa - 16729-031-01 - (Methyldopa)
Drug Information of Methyldopa
| Product NDC: | 16729-031 |
| Proprietary Name: | Methyldopa |
| Non Proprietary Name: | Methyldopa |
| Active Ingredient(s): | 500 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: | 16729-031 |
| Labeler Name: | Accord Healthcare Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070085 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120627 |
Package Information of Methyldopa
| Package NDC: | 16729-031-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (16729-031-01) |
NDC Information of Methyldopa
| NDC Code | 16729-031-01 |
| Proprietary Name | Methyldopa |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (16729-031-01) |
| Product NDC | 16729-031 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methyldopa |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120627 |
| Marketing Category Name | ANDA |
| Labeler Name | Accord Healthcare Inc. |
| Substance Name | METHYLDOPA |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
