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GILTUSS TOTAL RELEASE
GILTUSS TOTAL RELEASE - 58552-317-01 - (Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl)
Drug Information of GILTUSS TOTAL RELEASE
| Product NDC: | 58552-317 |
| Proprietary Name: | GILTUSS TOTAL RELEASE |
| Non Proprietary Name: | Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl |
| Active Ingredient(s): | 28; 388; 10 mg/1; mg/1; mg/1 & nbsp; Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GILTUSS TOTAL RELEASE
| Product NDC: | 58552-317 |
| 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 TOTAL RELEASE
| Package NDC: | 58552-317-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (58552-317-01) |
NDC Information of GILTUSS TOTAL RELEASE
| NDC Code | 58552-317-01 |
| Proprietary Name | GILTUSS TOTAL RELEASE |
| Package Description | 100 TABLET in 1 BOTTLE (58552-317-01) |
| Product NDC | 58552-317 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Dextromethorphan HBr, and Phenylephrine HCl |
| Dosage Form Name | TABLET |
| 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/1; mg/1; mg/1 |
| Pharmaceutical Classes |
