POLY-TUSSIN - Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin
Navigation: NDC > Supplier starting with: P > POLY PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 50991-529 |
| Proprietary Name: | POLY-TUSSIN |
| Suffix: | EX |
| Non-Proprietary Name: | Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin |
| Dosage Form: | SYRUP |
| Method: | ORAL |
| Original Marketing Date: | 16-11-2009 |
| Category Name: | UNAPPROVED DRUG OTHER |
| Application Number: | |
| Labeler: | POLY PHARMACEUTICALS, INC. |
| Substance Name: | DIHYDROCODEINE BITARTRATE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Numerator Strength: | 7.5; 50; 5 |
| Active Ingredient Unit: | mg/5mL; mg/5mL; mg/5mL |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CIII |