Home
>
National Drug Code (NDC)
>
GILTUSS PEDIATRIC
GILTUSS PEDIATRIC - 58552-121-02 - (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)
Drug Information of GILTUSS PEDIATRIC
| 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) |
Labeler Information of GILTUSS PEDIATRIC
| 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 Information of GILTUSS PEDIATRIC
| Package NDC: | 58552-121-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (58552-121-02) > 60 mL in 1 BOTTLE |
NDC Information of GILTUSS PEDIATRIC
| 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 |
