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Bionatuss
Bionatuss - 45737-210-16 - (Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine)
Drug Information of Bionatuss
| Product NDC: | 45737-210 |
| Proprietary Name: | Bionatuss |
| Non Proprietary Name: | Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine |
| Active Ingredient(s): | 2; 20; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dexbrompheniramine Maleate, Dextromethorphan, Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bionatuss
| Product NDC: | 45737-210 |
| 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 Bionatuss
| Package NDC: | 45737-210-16 |
| Package Description: | 473 mL in 1 BOTTLE (45737-210-16) |
NDC Information of Bionatuss
| NDC Code | 45737-210-16 |
| Proprietary Name | Bionatuss |
| Package Description | 473 mL in 1 BOTTLE (45737-210-16) |
| Product NDC | 45737-210 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dexbrompheniramine Maleate, Dextromethorphan, 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 | DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 20; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
