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BioGtuss
BioGtuss - 45737-205-16 - (Dextromethorphan, Guaifenesin, Phenylephrine)
Drug Information of BioGtuss
| Product NDC: | 45737-205 |
| Proprietary Name: | BioGtuss |
| Non Proprietary Name: | Dextromethorphan, Guaifenesin, Phenylephrine |
| Active Ingredient(s): | 15; 300; 15 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan, Guaifenesin, Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BioGtuss
| Product NDC: | 45737-205 |
| Labeler Name: | Advanced Generic Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091001 |
Package Information of BioGtuss
| Package NDC: | 45737-205-16 |
| Package Description: | 473 mL in 1 BOTTLE (45737-205-16) |
NDC Information of BioGtuss
| NDC Code | 45737-205-16 |
| Proprietary Name | BioGtuss |
| Package Description | 473 mL in 1 BOTTLE (45737-205-16) |
| Product NDC | 45737-205 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan, Guaifenesin, Phenylephrine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advanced Generic Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 15; 300; 15 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
