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 |