Product NDC: | 52083-600 |
Proprietary Name: | G-ZYNCOF |
Non Proprietary Name: | Dextromethorphan HBr and Guaifenesin |
Active Ingredient(s): | 20; 400 mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr and Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52083-600 |
Labeler Name: | Kramer Novis |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121203 |
Package NDC: | 52083-600-16 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (52083-600-16) |
NDC Code | 52083-600-16 |
Proprietary Name | G-ZYNCOF |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (52083-600-16) |
Product NDC | 52083-600 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr and Guaifenesin |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20121203 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kramer Novis |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 20; 400 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |