Product NDC: | 59779-442 |
Proprietary Name: | Long Acting Tussin Cough Gels |
Non Proprietary Name: | Dextromethorphan HBr |
Active Ingredient(s): | 15 mg/1 & nbsp; Dextromethorphan HBr |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-442 |
Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060424 |
Package NDC: | 59779-442-09 |
Package Description: | 1 BOTTLE in 1 PACKAGE (59779-442-09) > 20 CAPSULE, GELATIN COATED in 1 BOTTLE |
NDC Code | 59779-442-09 |
Proprietary Name | Long Acting Tussin Cough Gels |
Package Description | 1 BOTTLE in 1 PACKAGE (59779-442-09) > 20 CAPSULE, GELATIN COATED in 1 BOTTLE |
Product NDC | 59779-442 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20060424 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes |