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Bisolvine
Bisolvine - 14505-389-04 - (Guaifenesin, Dextromethorphan)
Drug Information of Bisolvine
| Product NDC: | 14505-389 |
| Proprietary Name: | Bisolvine |
| Non Proprietary Name: | Guaifenesin, Dextromethorphan |
| Active Ingredient(s): | 100; 10 mg/5mL; mg/5mL & nbsp; Guaifenesin, Dextromethorphan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bisolvine
| Product NDC: | 14505-389 |
| Labeler Name: | Pharmalab Enterprises Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100218 |
Package Information of Bisolvine
| Package NDC: | 14505-389-04 |
| Package Description: | 120 mL in 1 BOTTLE, PLASTIC (14505-389-04) |
NDC Information of Bisolvine
| NDC Code | 14505-389-04 |
| Proprietary Name | Bisolvine |
| Package Description | 120 mL in 1 BOTTLE, PLASTIC (14505-389-04) |
| Product NDC | 14505-389 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Dextromethorphan |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100218 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pharmalab Enterprises Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 100; 10 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
