Product NDC: | 54859-602 |
Proprietary Name: | Tusnel Pediatric |
Non Proprietary Name: | Guiafenesin, Pseudoephedrine HCl |
Active Ingredient(s): | 25; 7.5 mg/mL; mg/mL & nbsp; Guiafenesin, Pseudoephedrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54859-602 |
Labeler Name: | Llorens Pharmaceutical International Division |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060101 |
Package NDC: | 54859-602-02 |
Package Description: | 60 mL in 1 BOTTLE, DROPPER (54859-602-02) |
NDC Code | 54859-602-02 |
Proprietary Name | Tusnel Pediatric |
Package Description | 60 mL in 1 BOTTLE, DROPPER (54859-602-02) |
Product NDC | 54859-602 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guiafenesin, Pseudoephedrine HCl |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20060101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Llorens Pharmaceutical International Division |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 25; 7.5 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |