Product NDC: | 0603-1550 |
Proprietary Name: | Povidone Iodine |
Non Proprietary Name: | povidone iodine |
Active Ingredient(s): | 100 mg/mL & nbsp; povidone iodine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-1550 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19950401 |
Package NDC: | 0603-1550-56 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (0603-1550-56) |
NDC Code | 0603-1550-56 |
Proprietary Name | Povidone Iodine |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (0603-1550-56) |
Product NDC | 0603-1550 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | povidone iodine |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19950401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | POVIDONE-IODINE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes |