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ACETAMINOPHEN and CODEINE
ACETAMINOPHEN and CODEINE - 43063-139-01 - (ACETAMINOPHEN and CODEINE)
Drug Information of ACETAMINOPHEN and CODEINE
| Product NDC: | 43063-139 |
| Proprietary Name: | ACETAMINOPHEN and CODEINE |
| Non Proprietary Name: | ACETAMINOPHEN and CODEINE |
| Active Ingredient(s): | 120; 12 mg/5mL; mg/5mL & nbsp; ACETAMINOPHEN and CODEINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACETAMINOPHEN and CODEINE
| Product NDC: | 43063-139 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040746 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of ACETAMINOPHEN and CODEINE
| Package NDC: | 43063-139-01 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (43063-139-01) |
NDC Information of ACETAMINOPHEN and CODEINE
| NDC Code | 43063-139-01 |
| Proprietary Name | ACETAMINOPHEN and CODEINE |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (43063-139-01) |
| Product NDC | 43063-139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ACETAMINOPHEN and CODEINE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 120; 12 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
