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Zephrex-D
Zephrex-D - 53240-151-01 - (Pseudoephedrine Hydrochloride)
Drug Information of Zephrex-D
| Product NDC: | 53240-151 |
| Proprietary Name: | Zephrex-D |
| Non Proprietary Name: | Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zephrex-D
| Product NDC: | 53240-151 |
| Labeler Name: | Westport Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121115 |
Package Information of Zephrex-D
| Package NDC: | 53240-151-01 |
| Package Description: | 24 TABLET in 1 PACKAGE (53240-151-01) |
NDC Information of Zephrex-D
| NDC Code | 53240-151-01 |
| Proprietary Name | Zephrex-D |
| Package Description | 24 TABLET in 1 PACKAGE (53240-151-01) |
| Product NDC | 53240-151 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Westport Pharmaceuticals |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
