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McKesson Nite Time
McKesson Nite Time - 49348-743-36 - (acetaminophen, dextromethorphan hydrobromide and doxylamine succinate)
Drug Information of McKesson Nite Time
| Product NDC: | 49348-743 |
| Proprietary Name: | McKesson Nite Time |
| 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 McKesson Nite Time
| Product NDC: | 49348-743 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090709 |
Package Information of McKesson Nite Time
| Package NDC: | 49348-743-36 |
| Package Description: | 177 mL in 1 BOTTLE (49348-743-36) |
NDC Information of McKesson Nite Time
| NDC Code | 49348-743-36 |
| Proprietary Name | McKesson Nite Time |
| Package Description | 177 mL in 1 BOTTLE (49348-743-36) |
| Product NDC | 49348-743 |
| 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 | 20090709 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
