Product NDC: | 64980-144 |
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) |
Product NDC: | 64980-144 |
Labeler Name: | Rising Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040723 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080402 |
Package NDC: | 64980-144-10 |
Package Description: | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-144-10) |
NDC Code | 64980-144-10 |
Proprietary Name | Isosorbide Dinitrate |
Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-144-10) |
Product NDC | 64980-144 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Isosorbide Dinitrate |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20080402 |
Marketing Category Name | ANDA |
Labeler Name | Rising Pharmaceuticals Inc |
Substance Name | ISOSORBIDE DINITRATE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes |