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ALAHIST
ALAHIST - 50991-814-16 - (Brompheniramine Maleate, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide)
Drug Information of ALAHIST
| Product NDC: | 50991-814 |
| Proprietary Name: | ALAHIST |
| Non Proprietary Name: | Brompheniramine Maleate, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 4; 15; 7.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Brompheniramine Maleate, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALAHIST
| Product NDC: | 50991-814 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071227 |
Package Information of ALAHIST
| Package NDC: | 50991-814-16 |
| Package Description: | 473 mL in 1 BOTTLE (50991-814-16) |
NDC Information of ALAHIST
| NDC Code | 50991-814-16 |
| Proprietary Name | ALAHIST |
| Package Description | 473 mL in 1 BOTTLE (50991-814-16) |
| Product NDC | 50991-814 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Brompheniramine Maleate, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20071227 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 15; 7.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
