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Giltuss
Giltuss - 58552-122-08 - (Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of Giltuss
| Product NDC: | 58552-122 |
| Proprietary Name: | Giltuss |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 28; 388; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Giltuss
| Product NDC: | 58552-122 |
| 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
| Package NDC: | 58552-122-08 |
| Package Description: | 237 mL in 1 BOTTLE (58552-122-08) |
NDC Information of Giltuss
| NDC Code | 58552-122-08 |
| Proprietary Name | Giltuss |
| Package Description | 237 mL in 1 BOTTLE (58552-122-08) |
| Product NDC | 58552-122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | SYRUP |
| 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 | 28; 388; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
