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Aldex AN
Aldex AN - 65224-542-01 - (DOXYLAMINE SUCCINATE)
Drug Information of Aldex AN
| Product NDC: | 65224-542 |
| Proprietary Name: | Aldex AN |
| Non Proprietary Name: | DOXYLAMINE SUCCINATE |
| Active Ingredient(s): | 5 mg/1 & nbsp; DOXYLAMINE SUCCINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aldex AN
| Product NDC: | 65224-542 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100120 |
Package Information of Aldex AN
| Package NDC: | 65224-542-01 |
| Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE (65224-542-01) |
NDC Information of Aldex AN
| NDC Code | 65224-542-01 |
| Proprietary Name | Aldex AN |
| Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE (65224-542-01) |
| Product NDC | 65224-542 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOXYLAMINE SUCCINATE |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20100120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | DOXYLAMINE SUCCINATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
