Product NDC: | 0363-0609 |
Proprietary Name: | Nighttime D |
Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride |
Active Ingredient(s): | 500; 15; 6.25; 30 mg/15mL; mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0609 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020628 |
Package NDC: | 0363-0609-38 |
Package Description: | 296 mL in 1 BOTTLE (0363-0609-38) |
NDC Code | 0363-0609-38 |
Proprietary Name | Nighttime D |
Package Description | 296 mL in 1 BOTTLE (0363-0609-38) |
Product NDC | 0363-0609 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20020628 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Walgreen Company |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 500; 15; 6.25; 30 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |