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Lusair
Lusair - 23359-017-16 - (Phenylephrine Hydrochloride and Guaifenesin)
Drug Information of Lusair
| Product NDC: | 23359-017 |
| Proprietary Name: | Lusair |
| Non Proprietary Name: | Phenylephrine Hydrochloride and Guaifenesin |
| Active Ingredient(s): | 200; 7.5 mg/5mL; mg/5mL & nbsp; Phenylephrine Hydrochloride and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lusair
| Product NDC: | 23359-017 |
| Labeler Name: | Centurion Labs, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110831 |
Package Information of Lusair
| Package NDC: | 23359-017-16 |
| Package Description: | 473 mL in 1 BOTTLE (23359-017-16) |
NDC Information of Lusair
| NDC Code | 23359-017-16 |
| Proprietary Name | Lusair |
| Package Description | 473 mL in 1 BOTTLE (23359-017-16) |
| Product NDC | 23359-017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride and Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110831 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Centurion Labs, LLC |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 200; 7.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
