Package 37808-126-35

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 37808-126-35
Digits Only 3780812635
Product NDC 37808-126
Description

1 BOTTLE in 1 BOTTLE (37808-126-35) / 35 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-06-15
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": "a08f35dd-f3d5-5689-c975-0ed213c90c7d", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["b13ab6fc-4fec-c870-2c5f-b5e31dec722a"], "manufacturer_name": ["HEB"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BLISTER PACK (37808-126-10)  / 5 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "37808-126-10", "marketing_start_date": "20190615"}, {"sample": false, "description": "1 BOTTLE in 1 BOTTLE (37808-126-35)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "37808-126-35", "marketing_start_date": "20190615"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-126-80)  / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "37808-126-80", "marketing_start_date": "20221001"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "37808-126_a08f35dd-f3d5-5689-c975-0ed213c90c7d", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-126", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210375", "marketing_category": "ANDA", "marketing_start_date": "20190615", "listing_expiration_date": "20271231"}