Product NDC: | 58552-121 |
Proprietary Name: | GILTUSS PEDIATRIC |
Non Proprietary Name: | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Active Ingredient(s): | 7.5; 88; 2.5 mg/mL; mg/mL; mg/mL & nbsp; dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58552-121 |
Labeler Name: | Gil Pharmaceutical Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091019 |
Package NDC: | 58552-121-02 |
Package Description: | 1 BOTTLE in 1 CARTON (58552-121-02) > 60 mL in 1 BOTTLE |
NDC Code | 58552-121-02 |
Proprietary Name | GILTUSS PEDIATRIC |
Package Description | 1 BOTTLE in 1 CARTON (58552-121-02) > 60 mL in 1 BOTTLE |
Product NDC | 58552-121 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20091019 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Gil Pharmaceutical Corp |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 7.5; 88; 2.5 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |