Package 68788-8282-1

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8282-1
Digits Only 6878882821
Product NDC 68788-8282
Product ID 68788-8282_a8280c67-17ed-48dd-98bd-2de50d34cc75
Description

1 BOTTLE in 1 CARTON (68788-8282-1) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-10-25
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": "a8280c67-17ed-48dd-98bd-2de50d34cc75", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["7e94be37-0971-44b3-9857-f56330d810b6"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-8282-1)  / 120 mL in 1 BOTTLE", "package_ndc": "68788-8282-1", "marketing_start_date": "20231025"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "68788-8282_a8280c67-17ed-48dd-98bd-2de50d34cc75", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-8282", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA076601", "marketing_category": "ANDA", "marketing_start_date": "20231025", "listing_expiration_date": "20261231"}