allergy relief

Generic: cetirizine hydrochloride

Labeler: chain drug consortium
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name cetirizine hydrochloride
Labeler chain drug consortium
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
CHAIN DRUG CONSORTIUM

Identifiers & Regulatory

Product NDC 68016-294
Product ID 68016-294_24340f37-44e4-b094-e063-6294a90a7886
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209274
Marketing Start 2019-11-01
Marketing End 2026-07-31

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 68016294
Hyphenated Format 68016-294

Supplemental Identifiers

RxCUI
1014678
UPC
0840986036255
UNII
64O047KTOA

Packaging Origin

Original Packager
true

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 allergy relief (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA209274 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-294-14) / 14 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-294-30) / 30 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-294-60) / 60 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (68016-294-90) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (4)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24340f37-44e4-b094-e063-6294a90a7886", "openfda": {"upc": ["0840986036255"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["5e0ef968-dff3-4446-8412-8085677332f0"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-294-14)  / 14 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-294-14", "marketing_end_date": "20260430", "marketing_start_date": "20191101"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-294-30)  / 30 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-294-30", "marketing_end_date": "20260731", "marketing_start_date": "20191101"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-294-60)  / 60 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-294-60", "marketing_end_date": "20260731", "marketing_start_date": "20191101"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-294-90)  / 90 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-294-90", "marketing_end_date": "20260731", "marketing_start_date": "20191101"}], "brand_name": "Allergy Relief", "product_id": "68016-294_24340f37-44e4-b094-e063-6294a90a7886", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68016-294", "generic_name": "Cetirizine hydrochloride", "labeler_name": "CHAIN DRUG CONSORTIUM", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20191101"}