| Product NDC: | 0603-7038 |
| Proprietary Name: | Acetic Acid |
| Non Proprietary Name: | Acetic Acid |
| Active Ingredient(s): | .02 mL/mL & nbsp; Acetic Acid |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0603-7038 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040607 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050224 |
| Package NDC: | 0603-7038-41 |
| Package Description: | 15 mL in 1 BOTTLE (0603-7038-41) |
| NDC Code | 0603-7038-41 |
| Proprietary Name | Acetic Acid |
| Package Description | 15 mL in 1 BOTTLE (0603-7038-41) |
| Product NDC | 0603-7038 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetic Acid |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20050224 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ACETIC ACID |
| Strength Number | .02 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |