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Suphedrine PE
Suphedrine PE - 70253-453-07 - (Phenylephrine HCl)
Drug Information of Suphedrine PE
| Product NDC: | 70253-453 |
| Proprietary Name: | Suphedrine PE |
| Non Proprietary Name: | Phenylephrine HCl |
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Suphedrine PE
| Product NDC: | 70253-453 |
| Labeler Name: | NASH-FINCH COMPANY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20041206 |
Package Information of Suphedrine PE
| Package NDC: | 70253-453-07 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (70253-453-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Suphedrine PE
| NDC Code | 70253-453-07 |
| Proprietary Name | Suphedrine PE |
| Package Description | 1 BLISTER PACK in 1 CARTON (70253-453-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 70253-453 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20041206 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NASH-FINCH COMPANY |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
