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Altipres
Altipres - 53163-104-16 - (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl)
Drug Information of Altipres
| Product NDC: | 53163-104 |
| Proprietary Name: | Altipres |
| Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 10; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Altipres
| Product NDC: | 53163-104 |
| Labeler Name: | Alternative Pharmacal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130501 |
Package Information of Altipres
| Package NDC: | 53163-104-16 |
| Package Description: | 473 mL in 1 BOTTLE (53163-104-16) |
NDC Information of Altipres
| NDC Code | 53163-104-16 |
| Proprietary Name | Altipres |
| Package Description | 473 mL in 1 BOTTLE (53163-104-16) |
| Product NDC | 53163-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Alternative Pharmacal Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
