Product NDC: | 0517-0740 |
Proprietary Name: | Methylergonovine Maleate |
Non Proprietary Name: | Methylergonovine Maleate |
Active Ingredient(s): | .2 mg/mL & nbsp; Methylergonovine Maleate |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-0740 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090193 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100621 |
Package NDC: | 0517-0740-20 |
Package Description: | 20 VIAL, SINGLE-DOSE in 1 CARTON (0517-0740-20) > 1 mL in 1 VIAL, SINGLE-DOSE (0517-0740-01) |
NDC Code | 0517-0740-20 |
Proprietary Name | Methylergonovine Maleate |
Package Description | 20 VIAL, SINGLE-DOSE in 1 CARTON (0517-0740-20) > 1 mL in 1 VIAL, SINGLE-DOSE (0517-0740-01) |
Product NDC | 0517-0740 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Methylergonovine Maleate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20100621 |
Marketing Category Name | ANDA |
Labeler Name | American Regent, Inc. |
Substance Name | METHYLERGONOVINE MALEATE |
Strength Number | .2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |