Package 69206-990-01

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69206-990-01
Digits Only 6920699001
Product NDC 69206-990
Product ID 69206-990_3e808491-ec96-4f20-bb5e-3a9e5c72550e
Description

120 mL in 1 BOTTLE (69206-990-01)

Marketing

Marketing Status
Marketed Since 2023-02-01
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e808491-ec96-4f20-bb5e-3a9e5c72550e", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["aeb73ab9-3b05-4062-a7fd-352cf2094a56"], "manufacturer_name": ["Aventura Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (69206-990-01)", "package_ndc": "69206-990-01", "marketing_start_date": "20230201"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "69206-990_3e808491-ec96-4f20-bb5e-3a9e5c72550e", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69206-990", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Aventura Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA078876", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}