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Cetirizine HCl and Pseudoephedrine HCl
Cetirizine HCl and Pseudoephedrine HCl - 63629-4399-1 - (Cetirizine HCl and Pseudoephedrine HCl)
Drug Information of Cetirizine HCl and Pseudoephedrine HCl
| Product NDC: | 63629-4399 |
| Proprietary Name: | Cetirizine HCl and Pseudoephedrine HCl |
| Non Proprietary Name: | Cetirizine HCl and Pseudoephedrine HCl |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; Cetirizine HCl and Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cetirizine HCl and Pseudoephedrine HCl
| Product NDC: | 63629-4399 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077991 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080305 |
Package Information of Cetirizine HCl and Pseudoephedrine HCl
| Package NDC: | 63629-4399-1 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4399-1) |
NDC Information of Cetirizine HCl and Pseudoephedrine HCl
| NDC Code | 63629-4399-1 |
| Proprietary Name | Cetirizine HCl and Pseudoephedrine HCl |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4399-1) |
| Product NDC | 63629-4399 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cetirizine HCl and Pseudoephedrine HCl |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080305 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
