| Product NDC: | 60432-741 |
| Proprietary Name: | Acetic Acid |
| Non Proprietary Name: | ACETIC ACID |
| Active Ingredient(s): | 25 mg/mL & nbsp; ACETIC ACID |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60432-741 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040166 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960726 |
| Package NDC: | 60432-741-15 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (60432-741-15) |
| NDC Code | 60432-741-15 |
| Proprietary Name | Acetic Acid |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (60432-741-15) |
| Product NDC | 60432-741 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ACETIC ACID |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 19960726 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | ACETIC ACID |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |