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Acetaminophen And Codeine
Acetaminophen And Codeine - 43063-014-04 - (acetaminophen and codeine phosphate)
Drug Information of Acetaminophen And Codeine
| Product NDC: | 43063-014 |
| Proprietary Name: | Acetaminophen And 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) |
Labeler Information of Acetaminophen And Codeine
| Product NDC: | 43063-014 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089805 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880930 |
Package Information of Acetaminophen And Codeine
| Package NDC: | 43063-014-04 |
| Package Description: | 4 TABLET in 1 BOTTLE, PLASTIC (43063-014-04) |
NDC Information of Acetaminophen And Codeine
| NDC Code | 43063-014-04 |
| Proprietary Name | Acetaminophen And Codeine |
| Package Description | 4 TABLET in 1 BOTTLE, PLASTIC (43063-014-04) |
| Product NDC | 43063-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen and codeine phosphate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19880930 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 300; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
