Package 68462-346-90

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 68462-346-90
Digits Only 6846234690
Product NDC 68462-346
Description

90 TABLET in 1 BOTTLE (68462-346-90)

Marketing

Marketing Status
Marketed Since 2011-02-25
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3dc84568-462c-4fca-b235-3a84f8a4bd7e", "openfda": {"upc": ["0368462346907"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["60ae7e0e-281c-40a3-a0d3-259b843ddaaa"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68462-346-90)", "package_ndc": "68462-346-90", "marketing_start_date": "20110225"}], "brand_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "product_id": "68462-346_3dc84568-462c-4fca-b235-3a84f8a4bd7e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68462-346", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "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": "20271231"}