| Product NDC: | 11584-1060 |
| Proprietary Name: | Despec |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 4; 20; 1.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11584-1060 |
| Labeler Name: | International Ethical Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080420 |
| Package NDC: | 11584-1060-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (11584-1060-1) > 30 mL in 1 BOTTLE |
| NDC Code | 11584-1060-1 |
| Proprietary Name | Despec |
| Package Description | 1 BOTTLE in 1 CARTON (11584-1060-1) > 30 mL in 1 BOTTLE |
| Product NDC | 11584-1060 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080420 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | International Ethical Laboratories |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 20; 1.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |