Home
>
National Drug Code (NDC)
>
Guaifenesin DM
Guaifenesin DM - 0121-4809-10 - (GUAIFENESIN and DEXTROMETHORPHAN)
Drug Information of Guaifenesin DM
| Product NDC: | 0121-4809 |
| Proprietary Name: | Guaifenesin DM |
| Non Proprietary Name: | GUAIFENESIN and DEXTROMETHORPHAN |
| Active Ingredient(s): | 10; 200 mg/5mL; mg/5mL & nbsp; GUAIFENESIN and DEXTROMETHORPHAN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin DM
| Product NDC: | 0121-4809 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100517 |
Package Information of Guaifenesin DM
| Package NDC: | 0121-4809-10 |
| Package Description: | 4 TRAY in 1 CASE (0121-4809-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
NDC Information of Guaifenesin DM
| NDC Code | 0121-4809-10 |
| Proprietary Name | Guaifenesin DM |
| Package Description | 4 TRAY in 1 CASE (0121-4809-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-4809 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and DEXTROMETHORPHAN |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20100517 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | DEXTROMETHORPHAN; GUAIFENESIN |
| Strength Number | 10; 200 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
