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NightTime
NightTime - 41268-041-30 - (acetaminophen, dextromethorphan hydrobromide and doxylamine succinate)
Drug Information of NightTime
| Product NDC: | 41268-041 |
| Proprietary Name: | NightTime |
| 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 NightTime
| Product NDC: | 41268-041 |
| Labeler Name: | Hannaford Brothers Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060621 |
Package Information of NightTime
| Package NDC: | 41268-041-30 |
| Package Description: | 177 mL in 1 BOTTLE (41268-041-30) |
NDC Information of NightTime
| NDC Code | 41268-041-30 |
| Proprietary Name | NightTime |
| Package Description | 177 mL in 1 BOTTLE (41268-041-30) |
| Product NDC | 41268-041 |
| 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 | 20060621 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hannaford Brothers Company |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
