Details for New Drug Application (NDA): 213557
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The generic ingredient in CETIRIZINE HYDROCHLORIDE is cetirizine hydrochloride; pseudoephedrine hydrochloride. There are thirty-nine drug master file entries for this compound. Twenty-six suppliers are listed for this compound. Additional details are available on the cetirizine hydrochloride; pseudoephedrine hydrochloride profile page.
Summary for 213557
Tradename: | CETIRIZINE HYDROCHLORIDE |
Applicant: | Aurobindo Pharma Ltd |
Ingredient: | cetirizine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 213557
Mechanism of Action | Histamine H1 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 213557
Suppliers and Packaging for NDA: 213557
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CETIRIZINE HYDROCHLORIDE | cetirizine hydrochloride | TABLET, ORALLY DISINTEGRATING;ORAL | 213557 | ANDA | WALGREEN CO. | 0363-0471 | 0363-0471-76 | 4 BLISTER PACK in 1 CARTON (0363-0471-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
CETIRIZINE HYDROCHLORIDE | cetirizine hydrochloride | TABLET, ORALLY DISINTEGRATING;ORAL | 213557 | ANDA | WALGREEN CO. | 0363-4025 | 0363-4025-76 | 4 BLISTER PACK in 1 CARTON (0363-4025-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 10MG | ||||
Approval Date: | Sep 11, 2020 | TE: | RLD: | No |
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