levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
levocetirizine dihydrochloride
Generic Name
levocetirizine dihydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
levocetirizine dihydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-023
Product ID
72789-023_2d58a1fb-47b6-e4c8-e063-6294a90ad5f3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091264
Listing Expiration
2026-12-31
Marketing Start
2012-06-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789023
Hyphenated Format
72789-023
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
levocetirizine dihydrochloride (source: ndc)
Generic Name
levocetirizine dihydrochloride (source: ndc)
Application Number
ANDA091264 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-023-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d58a1fb-47b6-e4c8-e063-6294a90ad5f3", "openfda": {"upc": ["0372789023304"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["57c7c673-790c-4158-87ca-7d8fb68c4286"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-023-30)", "package_ndc": "72789-023-30", "marketing_start_date": "20191017"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "72789-023_2d58a1fb-47b6-e4c8-e063-6294a90ad5f3", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72789-023", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20120629", "listing_expiration_date": "20261231"}