Package 51655-148-52

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-148-52
Digits Only 5165514852
Product NDC 51655-148
Product ID 51655-148_499e8a3e-9b27-9655-e063-6294a90a3be8
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-148-52)

Marketing

Marketing Status
Marketed Since 2022-10-04
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": "499e8a3e-9b27-9655-e063-6294a90a3be8", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["f2b458d6-ac10-0fed-e053-2a95a90a0f9c"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-148-52)", "package_ndc": "51655-148-52", "marketing_start_date": "20221004"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "51655-148_499e8a3e-9b27-9655-e063-6294a90a3be8", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51655-148", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091264", "marketing_category": "ANDA", "marketing_start_date": "20221004", "listing_expiration_date": "20271231"}