allergy relief-d

Generic: cetirizine hydrochloride and pseudoephedrine hydrochloride

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

Drug Facts

Product Profile

Brand Name allergy relief-d
Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride
Labeler chain drug consortium,llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 5 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer
CHAIN DRUG CONSORTIUM,LLC

Identifiers & Regulatory

Product NDC 68016-531
Product ID 68016-531_d2448d3f-a6f0-47c9-bf63-0a4bcdaf0ae4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA090922
Listing Expiration 2026-12-31
Marketing Start 2016-08-17

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68016531
Hyphenated Format 68016-531

Supplemental Identifiers

RxCUI
1014571
UNII
64O047KTOA 6V9V2RYJ8N

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-d (source: ndc)
Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA090922 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (68016-531-24)
source: ndc

Packages (1)

68016-531-24 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (68016-531-24)

Ingredients (2)

cetirizine hydrochloride (5 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

Allergy relief-D ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d2448d3f-a6f0-47c9-bf63-0a4bcdaf0ae4", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["0f5de86d-1c87-4664-83f6-4c17f78f7d35"], "manufacturer_name": ["CHAIN DRUG CONSORTIUM,LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (68016-531-24)", "package_ndc": "68016-531-24", "marketing_start_date": "20160817"}], "brand_name": "Allergy relief-D", "product_id": "68016-531_d2448d3f-a6f0-47c9-bf63-0a4bcdaf0ae4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "68016-531", "generic_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "CHAIN DRUG CONSORTIUM,LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy relief-D", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090922", "marketing_category": "ANDA", "marketing_start_date": "20160817", "listing_expiration_date": "20261231"}