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Pediatex
Pediatex - 65224-539-30 - (TRIPROLIDINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE)
Drug Information of Pediatex
| Product NDC: | 65224-539 |
| Proprietary Name: | Pediatex |
| Non Proprietary Name: | TRIPROLIDINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Ingredient(s): | 10; .938 mg/mL; mg/mL & nbsp; TRIPROLIDINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pediatex
| Product NDC: | 65224-539 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091020 |
Package Information of Pediatex
| Package NDC: | 65224-539-30 |
| Package Description: | 1 BOTTLE in 1 BOX (65224-539-30) > 30 mL in 1 BOTTLE |
NDC Information of Pediatex
| NDC Code | 65224-539-30 |
| Proprietary Name | Pediatex |
| Package Description | 1 BOTTLE in 1 BOX (65224-539-30) > 30 mL in 1 BOTTLE |
| Product NDC | 65224-539 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRIPROLIDINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20091020 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE |
| Strength Number | 10; .938 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
