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IMDUR
IMDUR - 0085-2028-01 - (isosorbide mononitrate)
Drug Information of IMDUR
| Product NDC: | 0085-2028 |
| Proprietary Name: | IMDUR |
| Non Proprietary Name: | isosorbide mononitrate |
| Active Ingredient(s): | 60 mg/1 & nbsp; isosorbide mononitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IMDUR
| Product NDC: | 0085-2028 |
| Labeler Name: | Schering Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075155 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060105 |
Package Information of IMDUR
| Package NDC: | 0085-2028-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-2028-01) |
NDC Information of IMDUR
| NDC Code | 0085-2028-01 |
| Proprietary Name | IMDUR |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-2028-01) |
| Product NDC | 0085-2028 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | isosorbide mononitrate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060105 |
| Marketing Category Name | ANDA |
| Labeler Name | Schering Corporation |
| Substance Name | ISOSORBIDE MONONITRATE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
