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Triadine
Triadine - 50730-8332-5 - (povidone-iodine)
Drug Information of Triadine
| Product NDC: | 50730-8332 |
| Proprietary Name: | Triadine |
| Non Proprietary Name: | povidone-iodine |
| Active Ingredient(s): | .075 mL/mL & nbsp; povidone-iodine |
| Administration Route(s): | EPIDURAL; PERCUTANEOUS; TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triadine
| Product NDC: | 50730-8332 |
| Labeler Name: | H and P Industries, Inc. dba Triad Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19850621 |
Package Information of Triadine
| Package NDC: | 50730-8332-5 |
| Package Description: | 946 mL in 1 BOTTLE (50730-8332-5) |
NDC Information of Triadine
| NDC Code | 50730-8332-5 |
| Proprietary Name | Triadine |
| Package Description | 946 mL in 1 BOTTLE (50730-8332-5) |
| Product NDC | 50730-8332 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | povidone-iodine |
| Dosage Form Name | SOLUTION |
| Route Name | EPIDURAL; PERCUTANEOUS; TOPICAL |
| Start Marketing Date | 19850621 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H and P Industries, Inc. dba Triad Group |
| Substance Name | POVIDONE-IODINE |
| Strength Number | .075 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
