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Aldex D
Aldex D - 65224-550-16 - (PHENYLEPHRINE HYDROCHLORIDE and PYRILAMINE MALEATE)
Drug Information of Aldex D
| Product NDC: | 65224-550 |
| Proprietary Name: | Aldex D |
| Non Proprietary Name: | PHENYLEPHRINE HYDROCHLORIDE and PYRILAMINE MALEATE |
| Active Ingredient(s): | 5; 16 mg/5mL; mg/5mL & nbsp; PHENYLEPHRINE HYDROCHLORIDE and PYRILAMINE MALEATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aldex D
| Product NDC: | 65224-550 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Aldex D
| Package NDC: | 65224-550-16 |
| Package Description: | 473 mL in 1 BOTTLE (65224-550-16) |
NDC Information of Aldex D
| NDC Code | 65224-550-16 |
| Proprietary Name | Aldex D |
| Package Description | 473 mL in 1 BOTTLE (65224-550-16) |
| Product NDC | 65224-550 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PHENYLEPHRINE HYDROCHLORIDE and PYRILAMINE MALEATE |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE |
| Strength Number | 5; 16 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
