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POLY-TUSSIN
POLY-TUSSIN - 50991-114-16 - (Chlorcyclizine Hydrochloride, Codeine Phosphate, Pseudoephedrine Hydrochloride)
Drug Information of POLY-TUSSIN
| Product NDC: | 50991-114 |
| Proprietary Name: | POLY-TUSSIN |
| Non Proprietary Name: | Chlorcyclizine Hydrochloride, Codeine Phosphate, Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 9.375; 10; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Chlorcyclizine Hydrochloride, Codeine Phosphate, Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of POLY-TUSSIN
| Product NDC: | 50991-114 |
| Labeler Name: | Poly Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120918 |
Package Information of POLY-TUSSIN
| Package NDC: | 50991-114-16 |
| Package Description: | 473 mL in 1 BOTTLE (50991-114-16) |
NDC Information of POLY-TUSSIN
| NDC Code | 50991-114-16 |
| Proprietary Name | POLY-TUSSIN |
| Package Description | 473 mL in 1 BOTTLE (50991-114-16) |
| Product NDC | 50991-114 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorcyclizine Hydrochloride, Codeine Phosphate, Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120918 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 9.375; 10; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
