| Product NDC: | 52083-620 |
| Proprietary Name: | Pecgen DMX |
| Non Proprietary Name: | guaifenesin,Dextromethorphan hydrobromide |
| Active Ingredient(s): | 15; 125 mg/5mL; mg/5mL & nbsp; guaifenesin,Dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52083-620 |
| Labeler Name: | KRAMER NOVIS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110329 |
| Package NDC: | 52083-620-16 |
| Package Description: | 480 mL in 1 BOTTLE (52083-620-16) |
| NDC Code | 52083-620-16 |
| Proprietary Name | Pecgen DMX |
| Package Description | 480 mL in 1 BOTTLE (52083-620-16) |
| Product NDC | 52083-620 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin,Dextromethorphan hydrobromide |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20110329 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KRAMER NOVIS |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 15; 125 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |