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Poly-Hist DM
Poly-Hist DM - 50991-220-16 - (Dextromethorphan Hydrobromide, Phenylephrine HCl and Thonzylamine HCl)
Drug Information of Poly-Hist DM
| Product NDC: | 50991-220 |
| Proprietary Name: | Poly-Hist DM |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Phenylephrine HCl and Thonzylamine HCl |
| Active Ingredient(s): | 10; 5; 25 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Phenylephrine HCl and Thonzylamine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Poly-Hist DM
| Product NDC: | 50991-220 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130622 |
Package Information of Poly-Hist DM
| Package NDC: | 50991-220-16 |
| Package Description: | 473 mL in 1 BOTTLE (50991-220-16) |
NDC Information of Poly-Hist DM
| NDC Code | 50991-220-16 |
| Proprietary Name | Poly-Hist DM |
| Package Description | 473 mL in 1 BOTTLE (50991-220-16) |
| Product NDC | 50991-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Phenylephrine HCl and Thonzylamine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130622 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; THONZYLAMINE HYDROCHLORIDE |
| Strength Number | 10; 5; 25 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
