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POLY-TUSSIN
POLY-TUSSIN - 50991-529-16 - (Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin)
Drug Information of POLY-TUSSIN
| Product NDC: | 50991-529 |
| Proprietary Name: | POLY-TUSSIN |
| Non Proprietary Name: | Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin |
| Active Ingredient(s): | 7.5; 50; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of POLY-TUSSIN
| Product NDC: | 50991-529 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091116 |
Package Information of POLY-TUSSIN
| Package NDC: | 50991-529-16 |
| Package Description: | 473 mL in 1 BOTTLE (50991-529-16) |
NDC Information of POLY-TUSSIN
| NDC Code | 50991-529-16 |
| Proprietary Name | POLY-TUSSIN |
| Package Description | 473 mL in 1 BOTTLE (50991-529-16) |
| Product NDC | 50991-529 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dihydrocodeine Bitartrate, Phenylephrine Hydrochloride, and Guaifenesin |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20091116 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | DIHYDROCODEINE BITARTRATE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 7.5; 50; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
