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Isosorbide Mononitrate
Isosorbide Mononitrate - 0143-1333-01 - (Isosorbide Mononitrate)
Drug Information of Isosorbide Mononitrate
| Product NDC: | 0143-1333 |
| Proprietary Name: | Isosorbide Mononitrate |
| Non Proprietary Name: | Isosorbide Mononitrate |
| Active Ingredient(s): | 20 mg/1 & nbsp; Isosorbide Mononitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isosorbide Mononitrate
| Product NDC: | 0143-1333 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075361 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20001005 |
Package Information of Isosorbide Mononitrate
| Package NDC: | 0143-1333-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE (0143-1333-01) |
NDC Information of Isosorbide Mononitrate
| NDC Code | 0143-1333-01 |
| Proprietary Name | Isosorbide Mononitrate |
| Package Description | 100 TABLET, COATED in 1 BOTTLE (0143-1333-01) |
| Product NDC | 0143-1333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosorbide Mononitrate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20001005 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | ISOSORBIDE MONONITRATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
