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ISOSORBIDE DINITRATE
ISOSORBIDE DINITRATE - 57664-600-88 - (ISOSORBIDE DINITRATE)
Drug Information of ISOSORBIDE DINITRATE
| Product NDC: | 57664-600 |
| Proprietary Name: | ISOSORBIDE DINITRATE |
| Non Proprietary Name: | ISOSORBIDE DINITRATE |
| Active Ingredient(s): | 40 mg/1 & nbsp; ISOSORBIDE DINITRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ISOSORBIDE DINITRATE
| Product NDC: | 57664-600 |
| Labeler Name: | Caraco Pharmaceutical Laboratories Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040009 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090922 |
Package Information of ISOSORBIDE DINITRATE
| Package NDC: | 57664-600-88 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-600-88) |
NDC Information of ISOSORBIDE DINITRATE
| NDC Code | 57664-600-88 |
| Proprietary Name | ISOSORBIDE DINITRATE |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-600-88) |
| Product NDC | 57664-600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ISOSORBIDE DINITRATE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090922 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories Ltd. |
| Substance Name | ISOSORBIDE DINITRATE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
