Package 68071-3841-9

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3841-9
Digits Only 6807138419
Product NDC 68071-3841
Product ID 68071-3841_348eadc6-98a0-06c0-e063-6394a90ae7ae
Description

90 TABLET in 1 BOTTLE (68071-3841-9)

Marketing

Marketing Status
Marketed Since 2025-05-07
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

LEVOCETIRIZINE DIHYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "348eadc6-98a0-06c0-e063-6394a90ae7ae", "openfda": {"upc": ["0368071384192"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["348eadb6-5be2-f8c7-e063-6394a90a1314"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3841-9)", "package_ndc": "68071-3841-9", "marketing_start_date": "20250507"}], "brand_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "product_id": "68071-3841_348eadc6-98a0-06c0-e063-6394a90ae7ae", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68071-3841", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOCETIRIZINE DIHYDROCHLORIDE", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090385", "marketing_category": "ANDA", "marketing_start_date": "20110225", "listing_expiration_date": "20261231"}