cetirizine hydrochloride

Generic: cetirizine hydrochloride

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cetirizine hydrochloride
Generic Name cetirizine hydrochloride
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-0790
Product ID 68788-0790_c3cc7ca5-7b22-4309-81ce-1b7326feb795
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077829
Listing Expiration 2026-12-31
Marketing Start 2009-10-01

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687880790
Hyphenated Format 68788-0790

Supplemental Identifiers

RxCUI
1014678
UNII
64O047KTOA

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 cetirizine hydrochloride (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA077829 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-0790-0)
  • 14 TABLET in 1 BOTTLE (68788-0790-1)
  • 30 TABLET in 1 BOTTLE (68788-0790-3)
  • 15 TABLET in 1 BOTTLE (68788-0790-5)
  • 60 TABLET in 1 BOTTLE (68788-0790-6)
  • 90 TABLET in 1 BOTTLE (68788-0790-9)
source: ndc

Packages (6)

68788-0790-0 100 TABLET in 1 BOTTLE (68788-0790-0) 68788-0790-1 14 TABLET in 1 BOTTLE (68788-0790-1) 68788-0790-3 30 TABLET in 1 BOTTLE (68788-0790-3) 68788-0790-5 15 TABLET in 1 BOTTLE (68788-0790-5) 68788-0790-6 60 TABLET in 1 BOTTLE (68788-0790-6) 68788-0790-9 90 TABLET in 1 BOTTLE (68788-0790-9)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Cetirizine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c3cc7ca5-7b22-4309-81ce-1b7326feb795", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["3fc53b32-704b-4586-aa8c-26a2a71a155a"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-0790-0)", "package_ndc": "68788-0790-0", "marketing_start_date": "20091001"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-0790-1)", "package_ndc": "68788-0790-1", "marketing_start_date": "20091001"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-0790-3)", "package_ndc": "68788-0790-3", "marketing_start_date": "20091001"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-0790-5)", "package_ndc": "68788-0790-5", "marketing_start_date": "20091001"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-0790-6)", "package_ndc": "68788-0790-6", "marketing_start_date": "20091001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-0790-9)", "package_ndc": "68788-0790-9", "marketing_start_date": "20091001"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "68788-0790_c3cc7ca5-7b22-4309-81ce-1b7326feb795", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-0790", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20091001", "listing_expiration_date": "20261231"}