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Betadine
Betadine - 0065-0411-30 - (povidone-iodine)
Drug Information of Betadine
| Product NDC: | 0065-0411 |
| Proprietary Name: | Betadine |
| Non Proprietary Name: | povidone-iodine |
| Active Ingredient(s): | 5 mg/mL & nbsp; povidone-iodine |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Betadine
| Product NDC: | 0065-0411 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018634 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000401 |
Package Information of Betadine
| Package NDC: | 0065-0411-30 |
| Package Description: | 30 mL in 1 BOTTLE (0065-0411-30) |
NDC Information of Betadine
| NDC Code | 0065-0411-30 |
| Proprietary Name | Betadine |
| Package Description | 30 mL in 1 BOTTLE (0065-0411-30) |
| Product NDC | 0065-0411 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | povidone-iodine |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20000401 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | POVIDONE-IODINE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
