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Povidone-Iodine
Povidone-Iodine - 0603-0599-50 - (povidone-iodine)
Drug Information of Povidone-Iodine
| Product NDC: | 0603-0599 |
| Proprietary Name: | Povidone-Iodine |
| Non Proprietary Name: | povidone-iodine |
| Active Ingredient(s): | 1 g/10g & nbsp; povidone-iodine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Povidone-Iodine
| Product NDC: | 0603-0599 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19970801 |
Package Information of Povidone-Iodine
| Package NDC: | 0603-0599-50 |
| Package Description: | 1 TUBE in 1 CARTON (0603-0599-50) > 28.4 g in 1 TUBE |
NDC Information of Povidone-Iodine
| NDC Code | 0603-0599-50 |
| Proprietary Name | Povidone-Iodine |
| Package Description | 1 TUBE in 1 CARTON (0603-0599-50) > 28.4 g in 1 TUBE |
| Product NDC | 0603-0599 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | povidone-iodine |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19970801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | POVIDONE-IODINE |
| Strength Number | 1 |
| Strength Unit | g/10g |
| Pharmaceutical Classes |
