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Non-Drowsy Suphedrine PE
Non-Drowsy Suphedrine PE - 49035-502-08 - (Acetaminophen and Phenylephrine HCl)
Drug Information of Non-Drowsy Suphedrine PE
| Product NDC: | 49035-502 |
| Proprietary Name: | Non-Drowsy Suphedrine PE |
| Non Proprietary Name: | Acetaminophen and Phenylephrine HCl |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; Acetaminophen and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Non-Drowsy Suphedrine PE
| Product NDC: | 49035-502 |
| Labeler Name: | Wal-Mart Stores Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050623 |
Package Information of Non-Drowsy Suphedrine PE
| Package NDC: | 49035-502-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49035-502-08) > 24 TABLET in 1 BLISTER PACK |
NDC Information of Non-Drowsy Suphedrine PE
| NDC Code | 49035-502-08 |
| Proprietary Name | Non-Drowsy Suphedrine PE |
| Package Description | 1 BLISTER PACK in 1 CARTON (49035-502-08) > 24 TABLET in 1 BLISTER PACK |
| Product NDC | 49035-502 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Phenylephrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050623 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wal-Mart Stores Inc |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
