Package 10135-639-90

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 10135-639-90
Digits Only 1013563990
Product NDC 10135-639
Product ID 10135-639_f380ef7e-eece-412d-b50c-deae2f6098d5
Description

90 TABLET, FILM COATED in 1 BOTTLE (10135-639-90)

Marketing

Marketing Status
Marketed Since 2018-09-01
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": "f380ef7e-eece-412d-b50c-deae2f6098d5", "openfda": {"upc": ["0310135639304", "0310135639908"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["f5d8d6a6-6455-430b-8923-090e1ca2ae3b"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (10135-639-30)", "package_ndc": "10135-639-30", "marketing_start_date": "20180901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (10135-639-90)", "package_ndc": "10135-639-90", "marketing_start_date": "20180901"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "10135-639_f380ef7e-eece-412d-b50c-deae2f6098d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "10135-639", "generic_name": "levocetirizine Dihydrochloride", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202046", "marketing_category": "ANDA", "marketing_start_date": "20180901", "listing_expiration_date": "20261231"}