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Codeine Sulfate
Codeine Sulfate - 54868-2541-0 - (codeine sulfate)
Drug Information of Codeine Sulfate
| Product NDC: | 54868-2541 |
| Proprietary Name: | Codeine Sulfate |
| Non Proprietary Name: | codeine sulfate |
| Active Ingredient(s): | 60 mg/1 & nbsp; codeine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Codeine Sulfate
| Product NDC: | 54868-2541 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022402 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090715 |
Package Information of Codeine Sulfate
| Package NDC: | 54868-2541-0 |
| Package Description: | 10 TABLET in 1 BOTTLE (54868-2541-0) |
NDC Information of Codeine Sulfate
| NDC Code | 54868-2541-0 |
| Proprietary Name | Codeine Sulfate |
| Package Description | 10 TABLET in 1 BOTTLE (54868-2541-0) |
| Product NDC | 54868-2541 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | codeine sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090715 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CODEINE SULFATE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
