| NDC Code | 0143-2260-10 |
|---|
| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0143-2260-10) |
|---|
| Product NDC | 0143-2260 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Isosorbide |
|---|
| Non-Proprietary Name | Isosorbide Mononitrate |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060330 |
|---|
| End Marketing Date | 20201231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076813 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | ISOSORBIDE MONONITRATE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE] |
|---|