Home
>
National Drug Code (NDC)
>
IOSAT
IOSAT - 51803-002-01 - (Potassium Iodide)
Drug Information of IOSAT
| Product NDC: | 51803-002 |
| Proprietary Name: | IOSAT |
| Non Proprietary Name: | Potassium Iodide |
| Active Ingredient(s): | 65 mg/1 & nbsp; Potassium Iodide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IOSAT
| Product NDC: | 51803-002 |
| Labeler Name: | Anbex Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA018664 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130501 |
Package Information of IOSAT
| Package NDC: | 51803-002-01 |
| Package Description: | 20 TABLET in 1 PACKAGE (51803-002-01) |
NDC Information of IOSAT
| NDC Code | 51803-002-01 |
| Proprietary Name | IOSAT |
| Package Description | 20 TABLET in 1 PACKAGE (51803-002-01) |
| Product NDC | 51803-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Iodide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | ANDA |
| Labeler Name | Anbex Inc. |
| Substance Name | POTASSIUM IODIDE |
| Strength Number | 65 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
