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 |