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DIGOXIN
DIGOXIN - 57664-441-88 - (DIGOXIN)
Drug Information of DIGOXIN
| Product NDC: | 57664-441 |
| Proprietary Name: | DIGOXIN |
| 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 DIGOXIN
| Product NDC: | 57664-441 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076363 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030731 |
Package Information of DIGOXIN
| Package NDC: | 57664-441-88 |
| Package Description: | 100 TABLET in 1 BOTTLE (57664-441-88) |
NDC Information of DIGOXIN
| NDC Code | 57664-441-88 |
| Proprietary Name | DIGOXIN |
| Package Description | 100 TABLET in 1 BOTTLE (57664-441-88) |
| Product NDC | 57664-441 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIGOXIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030731 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | DIGOXIN |
| Strength Number | 250 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient] |
