Cetirizine Hydrochloride
Cetirizine Hydrochloride Oral Solution, USP
Approved
Approval ID
2e2675ed-bcba-4ebc-99a7-2df6020db748
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 12, 2022
Manufacturers
FDA
Breckenridge Pharmaceutical, Inc.
DUNS: 150554335
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cetirizine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51991-837
Application NumberANDA078488
Product Classification
M
Marketing Category
C73584
G
Generic Name
Cetirizine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJuly 12, 2022
FDA Product Classification
INGREDIENTS (11)
Cetirizine HydrochlorideActive
Quantity: 1 mg in 1 mL
Code: 64O047KTOA
Classification: ACTIB
bananaInactive
Code: 4AJZ4765R9
Classification: IACT
glycerinInactive
Code: PDC6A3C0OX
Classification: IACT
methylparabenInactive
Code: A2I8C7HI9T
Classification: IACT
acetic acidInactive
Code: Q40Q9N063P
Classification: IACT
propylene glycolInactive
Code: 6DC9Q167V3
Classification: IACT
sodium acetateInactive
Code: 4550K0SC9B
Classification: IACT
propylparabenInactive
Code: Z8IX2SC1OH
Classification: IACT
sucroseInactive
Code: C151H8M554
Classification: IACT
grapeInactive
Code: 6X543N684K
Classification: IACT
waterInactive
Code: 059QF0KO0R
Classification: IACT