Details for New Drug Application (NDA): 210375
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The generic ingredient in LEVOCETIRIZINE DIHYDROCHLORIDE is levocetirizine dihydrochloride. There are thirteen drug master file entries for this compound. Fifty suppliers are listed for this compound. Additional details are available on the levocetirizine dihydrochloride profile page.
Summary for 210375
Tradename: | LEVOCETIRIZINE DIHYDROCHLORIDE |
Applicant: | Dr Reddys |
Ingredient: | levocetirizine dihydrochloride |
Patents: | 0 |
Pharmacology for NDA: 210375
Mechanism of Action | Histamine H1 Receptor Antagonists |
Suppliers and Packaging for NDA: 210375
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LEVOCETIRIZINE DIHYDROCHLORIDE | levocetirizine dihydrochloride | TABLET;ORAL | 210375 | ANDA | Walgreens Company | 0363-5529 | 0363-5529-10 | 2 BLISTER PACK in 1 CARTON (0363-5529-10) / 5 TABLET, COATED in 1 BLISTER PACK |
LEVOCETIRIZINE DIHYDROCHLORIDE | levocetirizine dihydrochloride | TABLET;ORAL | 210375 | ANDA | Walgreens Company | 0363-5529 | 0363-5529-12 | 1 BOTTLE in 1 CARTON (0363-5529-12) / 120 TABLET, COATED in 1 BOTTLE |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Jan 19, 2018 | TE: | RLD: | No |
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