Zodryl DEC 50 (CodaDose, Inc.)
Welcome to the PulseAid listing for the Zodryl DEC 50 drug offered from CodaDose, 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: | CodaDose, Inc. |
NON-PROPRIETARY NAME: | codeine phosphate, guaifenesin and pseudoephedrine hydrochloride |
SUBSTANCE NAME: | PSEUDOEPHEDRINE HYDROCHLORIDE; CODEINE PHOSPHATE; GUAIFENESIN |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | SUSPENSION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2009-08-24 |
END MARKETING DATE: | 0000-00-00 |
Zodryl DEC 50 HUMAN OTC DRUG Details:
Item Description | Zodryl DEC 50 from CodaDose, Inc. |
LABELER NAME: | CodaDose, Inc. |
DEA SCHEDULE: | CV
|
ACTIVE STRENGTH: | 30; 5; 100(mg/5mL; mg/5mL; mg/5mL) |
START MARKETING DATE: | 2009-08-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 43378-124_5ace705f-df68-4517-b65a-06c468111906 |
PRODUCT NDC: | 43378-124 |
APPLICATION NUMBER: | part341 |
Other PSEUDOEPHEDRINE HYDROCHLORIDE; CODEINE PHOSPHATE; GUAIFENESIN Pharmaceutical Manufacturers / Labelers: