| 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 |