Details for New Drug Application (NDA): 076047
✉ Email this page to a colleague
The generic ingredient in CETIRIZINE HYDROCHLORIDE ALLERGY is cetirizine hydrochloride. There are thirty-nine drug master file entries for this compound. One hundred and sixty suppliers are listed for this compound. Additional details are available on the cetirizine hydrochloride profile page.
Summary for 076047
| Tradename: | CETIRIZINE HYDROCHLORIDE ALLERGY |
| Applicant: | Contract Pharmacal |
| Ingredient: | cetirizine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 076047
| Mechanism of Action | Histamine H1 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 076047
Suppliers and Packaging for NDA: 076047
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CETIRIZINE HYDROCHLORIDE ALLERGY | cetirizine hydrochloride | TABLET;ORAL | 076047 | ANDA | Contract Pharmacal Corp. | 10267-3579 | 10267-3579-1 | 1 BOTTLE in 1 CARTON (10267-3579-1) / 100 TABLET, FILM COATED in 1 BOTTLE |
| CETIRIZINE HYDROCHLORIDE ALLERGY | cetirizine hydrochloride | TABLET;ORAL | 076047 | ANDA | Contract Pharmacal Corp. | 10267-3579 | 10267-3579-3 | 1 BOTTLE in 1 CARTON (10267-3579-3) / 30 TABLET, FILM COATED in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | Dec 27, 2007 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Dec 27, 2007 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
