Product NDC: | 55154-1908 |
Proprietary Name: | TYLENOL with Codeine |
Non Proprietary Name: | acetaminophen and codeine phosphate |
Active Ingredient(s): | 300; 30 mg/1; mg/1 & nbsp; acetaminophen and codeine phosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1908 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085055 |
Marketing Category: | ANDA |
Start Marketing Date: | 19820101 |
Package NDC: | 55154-1908-1 |
Package Description: | 100 TABLET in 1 BOTTLE (55154-1908-1) |
NDC Code | 55154-1908-1 |
Proprietary Name | TYLENOL with Codeine |
Package Description | 100 TABLET in 1 BOTTLE (55154-1908-1) |
Product NDC | 55154-1908 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | acetaminophen and codeine phosphate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19820101 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength Number | 300; 30 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |