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NITETIME
NITETIME - 56062-668-38 - (Dextromethorphan Hydrobromide, Doxylamine Succinate)
Drug Information of NITETIME
| Product NDC: | 56062-668 |
| Proprietary Name: | NITETIME |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Active Ingredient(s): | 15; 6.25 mg/15mL; mg/15mL & nbsp; Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NITETIME
| Product NDC: | 56062-668 |
| Labeler Name: | Publix Super Markets Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030120 |
Package Information of NITETIME
| Package NDC: | 56062-668-38 |
| Package Description: | 296 mL in 1 BOTTLE (56062-668-38) |
NDC Information of NITETIME
| NDC Code | 56062-668-38 |
| Proprietary Name | NITETIME |
| Package Description | 296 mL in 1 BOTTLE (56062-668-38) |
| Product NDC | 56062-668 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20030120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Publix Super Markets Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL |
| Pharmaceutical Classes |
