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Fexofenadine HCl and Pseudoephedrine HCI
Fexofenadine HCl and Pseudoephedrine HCI - 55111-557-35 - (Fexofenadine HCl and Pseudoephedrine HCI)
Drug Information of Fexofenadine HCl and Pseudoephedrine HCI
| Product NDC: | 55111-557 |
| Proprietary Name: | Fexofenadine HCl and Pseudoephedrine HCI |
| Non Proprietary Name: | Fexofenadine HCl and Pseudoephedrine HCI |
| Active Ingredient(s): | 180; 240 mg/1; mg/1 & nbsp; Fexofenadine HCl and Pseudoephedrine HCI |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine HCl and Pseudoephedrine HCI
| Product NDC: | 55111-557 |
| Labeler Name: | Dr.Reddy's Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079043 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110824 |
Package Information of Fexofenadine HCl and Pseudoephedrine HCI
| Package NDC: | 55111-557-35 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (55111-557-35) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Fexofenadine HCl and Pseudoephedrine HCI
| NDC Code | 55111-557-35 |
| Proprietary Name | Fexofenadine HCl and Pseudoephedrine HCI |
| Package Description | 2 BLISTER PACK in 1 CARTON (55111-557-35) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 55111-557 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fexofenadine HCl and Pseudoephedrine HCI |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110824 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 180; 240 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
