Product NDC: | 60760-036 |
Proprietary Name: | ISOSORBIDE MONONITRATE |
Non Proprietary Name: | ISOSORBIDE MONONITRATE |
Active Ingredient(s): | 30 mg/1 & nbsp; ISOSORBIDE MONONITRATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-036 |
Labeler Name: | St Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075155 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130515 |
Package NDC: | 60760-036-30 |
Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-036-30) |
NDC Code | 60760-036-30 |
Proprietary Name | ISOSORBIDE MONONITRATE |
Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-036-30) |
Product NDC | 60760-036 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ISOSORBIDE MONONITRATE |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20130515 |
Marketing Category Name | ANDA |
Labeler Name | St Marys Medical Park Pharmacy |
Substance Name | ISOSORBIDE MONONITRATE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |