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All-Nite Cold and Flu
All-Nite Cold and Flu - 0904-5777-21 - (acetaminophen, dextromethorphan hydrobromide and doxylamine succinate)
Drug Information of All-Nite Cold and Flu
| Product NDC: | 0904-5777 |
| Proprietary Name: | All-Nite Cold and Flu |
| Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All-Nite Cold and Flu
| Product NDC: | 0904-5777 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090218 |
Package Information of All-Nite Cold and Flu
| Package NDC: | 0904-5777-21 |
| Package Description: | 177 mL in 1 BOTTLE (0904-5777-21) |
NDC Information of All-Nite Cold and Flu
| NDC Code | 0904-5777-21 |
| Proprietary Name | All-Nite Cold and Flu |
| Package Description | 177 mL in 1 BOTTLE (0904-5777-21) |
| Product NDC | 0904-5777 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090218 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
