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DIGOX
DIGOX - 49349-797-20 - (Digoxin)
Drug Information of DIGOX
| Product NDC: | 49349-797 |
| Proprietary Name: | DIGOX |
| Non Proprietary Name: | Digoxin |
| Active Ingredient(s): | 250 ug/1 & nbsp; Digoxin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIGOX
| Product NDC: | 49349-797 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076268 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130305 |
Package Information of DIGOX
| Package NDC: | 49349-797-20 |
| Package Description: | 100 TABLET in 1 VIAL (49349-797-20) |
NDC Information of DIGOX
| NDC Code | 49349-797-20 |
| Proprietary Name | DIGOX |
| Package Description | 100 TABLET in 1 VIAL (49349-797-20) |
| Product NDC | 49349-797 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Digoxin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130305 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DIGOXIN |
| Strength Number | 250 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |
