GUAIFENESIN DM is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Guaifenesin; Dextromethorphan.
| Product ID | 50090-2303_203f3aee-0970-46b7-b40f-abfb548ff04b |
| NDC | 50090-2303 |
| Product Type | Human Otc Drug |
| Proprietary Name | GUAIFENESIN DM |
| Generic Name | Guaifenesin And Dextromethorphan |
| Dosage Form | Syrup |
| Route of Administration | ORAL |
| Marketing Start Date | 1992-07-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | A-S Medication Solutions |
| Substance Name | GUAIFENESIN; DEXTROMETHORPHAN |
| Active Ingredient Strength | 100 mg/5mL; mg/5mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2016-02-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-02-12 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 100 mg/5mL |
| SPL SET ID: | b6ea7ce0-a526-4cb1-848b-84573f4e8154 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0121-0638 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-0809 | Guaifenesin DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-1276 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 0121-4809 | Guaifenesin DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 43063-801 | Guaifenesin DM | Guaifenesin and Dextromethorphan Hydrobromide |
| 50090-2303 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 50090-3492 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 55154-5783 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 55154-5785 | GUAIFENESIN DM | GUAIFENESIN and DEXTROMETHORPHAN |
| 66007-204 | Expectorant plus Cough Relief | Guaifenesin and Dextromethorphan |
| 69822-021 | MMM - Cough Formula Guaifenesin DM | Guaifenesin DM |