| Product NDC: | 55154-9415 |
| Proprietary Name: | Acetaminophen and Codeine Phosphate |
| Non Proprietary Name: | Acetaminophen and Codeine Phosphate |
| Active Ingredient(s): | 120; 12 mg/5mL; mg/5mL & nbsp; Acetaminophen and Codeine Phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-9415 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087508 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110610 |
| Package NDC: | 55154-9415-5 |
| Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9415-5) > 5 mL in 1 CUP, UNIT-DOSE |
| NDC Code | 55154-9415-5 |
| Proprietary Name | Acetaminophen and Codeine Phosphate |
| Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9415-5) > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55154-9415 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetaminophen and Codeine Phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110610 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 120; 12 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |