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Methyldopate Hydrochloride
Methyldopate Hydrochloride - 0517-8905-10 - (Methyldopate Hydrochloride)
Drug Information of Methyldopate Hydrochloride
| Product NDC: | 0517-8905 |
| Proprietary Name: | Methyldopate Hydrochloride |
| Non Proprietary Name: | Methyldopate Hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Methyldopate Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methyldopate Hydrochloride
| Product NDC: | 0517-8905 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071279 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950930 |
Package Information of Methyldopate Hydrochloride
| Package NDC: | 0517-8905-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-8905-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Methyldopate Hydrochloride
| NDC Code | 0517-8905-10 |
| Proprietary Name | Methyldopate Hydrochloride |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-8905-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-8905 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methyldopate Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19950930 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | METHYLDOPATE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
