Product NDC: | 12634-526 |
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: | 12634-526 |
Labeler Name: | Apotheca, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089805 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020503 |
Package NDC: | 12634-526-85 |
Package Description: | 15 TABLET in 1 BOTTLE (12634-526-85) |
NDC Code | 12634-526-85 |
Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
Package Description | 15 TABLET in 1 BOTTLE (12634-526-85) |
Product NDC | 12634-526 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ACETAMINOPHEN AND CODEINE PHOSPHATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20020503 |
Marketing Category Name | ANDA |
Labeler Name | Apotheca, Inc. |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength Number | 300; 30 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |