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Aldex
Aldex - 65224-557-01 - (PSEUDOEPHEDRINE HYDROCHLORIDE and GUAIFENESIN)
Drug Information of Aldex
| Product NDC: | 65224-557 |
| Proprietary Name: | Aldex |
| Non Proprietary Name: | PSEUDOEPHEDRINE HYDROCHLORIDE and GUAIFENESIN |
| Active Ingredient(s): | 190; 30 mg/1; mg/1 & nbsp; PSEUDOEPHEDRINE HYDROCHLORIDE and GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aldex
| Product NDC: | 65224-557 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110321 |
Package Information of Aldex
| Package NDC: | 65224-557-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (65224-557-01) |
NDC Information of Aldex
| NDC Code | 65224-557-01 |
| Proprietary Name | Aldex |
| Package Description | 100 TABLET in 1 BOTTLE (65224-557-01) |
| Product NDC | 65224-557 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PSEUDOEPHEDRINE HYDROCHLORIDE and GUAIFENESIN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110321 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 190; 30 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
