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Diovan
Diovan - 21695-917-90 - (valsartan)
Drug Information of Diovan
| Product NDC: | 21695-917 |
| Proprietary Name: | Diovan |
| Non Proprietary Name: | valsartan |
| Active Ingredient(s): | 80 mg/1 & nbsp; valsartan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diovan
| Product NDC: | 21695-917 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021283 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010701 |
Package Information of Diovan
| Package NDC: | 21695-917-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-917-90) |
NDC Information of Diovan
| NDC Code | 21695-917-90 |
| Proprietary Name | Diovan |
| Package Description | 90 TABLET in 1 BOTTLE (21695-917-90) |
| Product NDC | 21695-917 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | valsartan |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010701 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | VALSARTAN |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
