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 | 50090-3492_487a929f-b905-42e5-8ded-cde745bfa370 |
NDC | 50090-3492 |
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 | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-06-20 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-06-20 |
Marketing End Date | 2019-09-30 |
Ingredient | Strength |
---|---|
GUAIFENESIN | 100 mg/5mL |
SPL SET ID: | 765e1568-2531-4731-a5e9-d1eea324cf16 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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 |