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Isosorbide mononitrate
Isosorbide mononitrate - 76237-192-30 - (Isosorbide mononitrate)
Drug Information of Isosorbide mononitrate
| Product NDC: | 76237-192 |
| Proprietary Name: | Isosorbide mononitrate |
| Non Proprietary Name: | Isosorbide mononitrate |
| Active Ingredient(s): | 60 mg/1 & nbsp; Isosorbide mononitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isosorbide mononitrate
| Product NDC: | 76237-192 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076813 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111128 |
Package Information of Isosorbide mononitrate
| Package NDC: | 76237-192-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-192-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Isosorbide mononitrate
| NDC Code | 76237-192-30 |
| Proprietary Name | Isosorbide mononitrate |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-192-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 76237-192 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosorbide mononitrate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111128 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | ISOSORBIDE MONONITRATE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
