| Product NDC: | 43063-329 |
| Proprietary Name: | methylergonovine maleate |
| Non Proprietary Name: | methylergonovine maleate |
| Active Ingredient(s): | .2 mg/1 & nbsp; methylergonovine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43063-329 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091577 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110801 |
| Package NDC: | 43063-329-08 |
| Package Description: | 8 TABLET in 1 BOTTLE, PLASTIC (43063-329-08) |
| NDC Code | 43063-329-08 |
| Proprietary Name | methylergonovine maleate |
| Package Description | 8 TABLET in 1 BOTTLE, PLASTIC (43063-329-08) |
| Product NDC | 43063-329 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylergonovine maleate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | METHYLERGONOVINE MALEATE |
| Strength Number | .2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |