Package 68788-8890-1

Brand: cetirizine hydrochloride oral solution

Generic: cetirizine hydrochloride oral solution
NDC Package

Package Facts

Identity

Package NDC 68788-8890-1
Digits Only 6878888901
Product NDC 68788-8890
Product ID 68788-8890_a03d33dc-a84c-4ab7-88a8-77333bfcb8e7
Description

120 mL in 1 BOTTLE (68788-8890-1)

Marketing

Marketing Status
Marketed Since 2025-06-27
Brand cetirizine hydrochloride oral solution
Generic cetirizine hydrochloride oral solution
Sample Package No

Linked Drug Pages (1)

Cetirizine Hydrochloride Oral Solution ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a03d33dc-a84c-4ab7-88a8-77333bfcb8e7", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["a03d33dc-a84c-4ab7-88a8-77333bfcb8e7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (68788-8890-1)", "package_ndc": "68788-8890-1", "marketing_start_date": "20250627"}], "brand_name": "Cetirizine Hydrochloride Oral Solution", "product_id": "68788-8890_a03d33dc-a84c-4ab7-88a8-77333bfcb8e7", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-8890", "generic_name": "Cetirizine Hydrochloride Oral Solution", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride Oral Solution", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA078870", "marketing_category": "ANDA", "marketing_start_date": "20250627", "listing_expiration_date": "20261231"}