Product NDC: | 49999-060 |
Proprietary Name: | ACETAMINOPHEN AND CODEINE PHOSPHATE |
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: | 49999-060 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040419 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111215 |
Package NDC: | 49999-060-20 |
Package Description: | 20 TABLET in 1 BOTTLE (49999-060-20) |
NDC Code | 49999-060-20 |
Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
Package Description | 20 TABLET in 1 BOTTLE (49999-060-20) |
Product NDC | 49999-060 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20111215 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength Number | 300; 30 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |