Product NDC: | 59365-6064 |
Proprietary Name: | Lugols Strong Iodine |
Non Proprietary Name: | Iodine Potassium Iodide |
Active Ingredient(s): | .05; .105 g/mL; g/mL & nbsp; Iodine Potassium Iodide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59365-6064 |
Labeler Name: | CooperSurgical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19921001 |
Package NDC: | 59365-6064-1 |
Package Description: | 12 VIAL, SINGLE-USE in 1 CARTON (59365-6064-1) > 8 mL in 1 VIAL, SINGLE-USE |
NDC Code | 59365-6064-1 |
Proprietary Name | Lugols Strong Iodine |
Package Description | 12 VIAL, SINGLE-USE in 1 CARTON (59365-6064-1) > 8 mL in 1 VIAL, SINGLE-USE |
Product NDC | 59365-6064 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Iodine Potassium Iodide |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19921001 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | CooperSurgical, Inc. |
Substance Name | IODINE; POTASSIUM IODIDE |
Strength Number | .05; .105 |
Strength Unit | g/mL; g/mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |