cetirizine hydrochloride

Generic: cetirizine hydrochloride tablets

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cetirizine hydrochloride
Generic Name cetirizine hydrochloride tablets
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-709
Product ID 71205-709_7e8d14d9-6d5a-4eb2-ac8a-0f84fe860020
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078343
Listing Expiration 2026-12-31
Marketing Start 2018-12-17

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 71205709
Hyphenated Format 71205-709

Supplemental Identifiers

RxCUI
1014678
UPC
0371205709068
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 tablets (source: ndc)
Application Number ANDA078343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00)
  • 6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90)
source: ndc

Packages (5)

71205-709-00 100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00) 71205-709-06 6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06) 71205-709-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10) 71205-709-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30) 71205-709-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90)

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": "7e8d14d9-6d5a-4eb2-ac8a-0f84fe860020", "openfda": {"upc": ["0371205709068"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["55b1738c-fa72-4cd1-a8e8-be41b12b593d"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00)", "package_ndc": "71205-709-00", "marketing_start_date": "20250708"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06)", "package_ndc": "71205-709-06", "marketing_start_date": "20221031"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10)", "package_ndc": "71205-709-10", "marketing_start_date": "20221031"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30)", "package_ndc": "71205-709-30", "marketing_start_date": "20221031"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90)", "package_ndc": "71205-709-90", "marketing_start_date": "20221031"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "71205-709_7e8d14d9-6d5a-4eb2-ac8a-0f84fe860020", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-709", "generic_name": "Cetirizine Hydrochloride Tablets", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078343", "marketing_category": "ANDA", "marketing_start_date": "20181217", "listing_expiration_date": "20261231"}