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Cocet Plus
Cocet Plus - 50991-312-05 - (acetaminophen and codeine phosphate)
Drug Information of Cocet Plus
| Product NDC: | 50991-312 |
| Proprietary Name: | Cocet Plus |
| Non Proprietary Name: | acetaminophen and codeine phosphate |
| Active Ingredient(s): | 650; 60 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 Cocet Plus
| Product NDC: | 50991-312 |
| Labeler Name: | Poly Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089363 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100629 |
Package Information of Cocet Plus
| Package NDC: | 50991-312-05 |
| Package Description: | 500 TABLET in 1 BOTTLE (50991-312-05) |
NDC Information of Cocet Plus
| NDC Code | 50991-312-05 |
| Proprietary Name | Cocet Plus |
| Package Description | 500 TABLET in 1 BOTTLE (50991-312-05) |
| Product NDC | 50991-312 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen and codeine phosphate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100629 |
| Marketing Category Name | ANDA |
| Labeler Name | Poly Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
| Strength Number | 650; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
