| Product NDC: | 49580-0408 |
| Proprietary Name: | Childrens Acetaminophen Oral Suspension |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49580-0408 |
| Labeler Name: | Aaron Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090729 |
| Package NDC: | 49580-0408-4 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (49580-0408-4) |
| NDC Code | 49580-0408-4 |
| Proprietary Name | Childrens Acetaminophen Oral Suspension |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (49580-0408-4) |
| Product NDC | 49580-0408 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090729 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Aaron Industries, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 160 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |