Coditussin DAC (Glendale Inc)
Welcome to the PulseAid listing for the Coditussin DAC drug offered from Glendale Inc. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Glendale Inc |
| NON-PROPRIETARY NAME: | CODEINE PHOSPHATE, GUAIFENESIN, and PSEUDOEPHEDRINE HYDROCHLORIDE |
| SUBSTANCE NAME: | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | SYRUP |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2016-05-01 |
| END MARKETING DATE: | 0000-00-00 |
Coditussin DAC HUMAN OTC DRUG Details:
| Item Description | Coditussin DAC from Glendale Inc |
| LABELER NAME: | Glendale Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 200; 30(mg/5mL; mg/5mL; mg/5mL) |
| START MARKETING DATE: | 2016-05-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70147-414_5a3c4507-724c-4145-8d32-be791e9c6fa4 |
| PRODUCT NDC: | 70147-414 |
| APPLICATION NUMBER: | part341 |
Other CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
