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Non-Drying Sinus PE
Non-Drying Sinus PE - 59779-548-08 - (Guaifenesin, Phenylephrine HCl)
Drug Information of Non-Drying Sinus PE
| Product NDC: | 59779-548 |
| Proprietary Name: | Non-Drying Sinus PE |
| Non Proprietary Name: | Guaifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 200; 5 mg/1; mg/1 & nbsp; Guaifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Non-Drying Sinus PE
| Product NDC: | 59779-548 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030917 |
Package Information of Non-Drying Sinus PE
| Package NDC: | 59779-548-08 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (59779-548-08) > 12 CAPSULE in 1 BLISTER PACK |
NDC Information of Non-Drying Sinus PE
| NDC Code | 59779-548-08 |
| Proprietary Name | Non-Drying Sinus PE |
| Package Description | 2 BLISTER PACK in 1 CARTON (59779-548-08) > 12 CAPSULE in 1 BLISTER PACK |
| Product NDC | 59779-548 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Phenylephrine HCl |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20030917 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 200; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
