fexofenadine hydrochloride and pseudoephedrine hydrochloride (69842-973)

Drug Facts

Product Profile

Brand Name fexofenadine hydrochloride and pseudoephedrine hydrochloride

Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride

Labeler cvs pharmacy

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

fexofenadine hydrochloride 60 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer

CVS Pharmacy

Identifiers & Regulatory

Product NDC 69842-973

Product ID 69842-973_136bd5d9-aea8-4a79-985d-35ddd01de47b

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA090818

Listing Expiration 2026-12-31

Marketing Start 2020-08-27

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 69842973

Hyphenated Format 69842-973

Supplemental Identifiers

RxCUI

997406

UNII

2S068B75ZU 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 fexofenadine hydrochloride and pseudoephedrine hydrochloride (source: ndc)

Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride (source: ndc)

Application Number ANDA090818 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

60 mg/1
120 mg/1

source: ndc

Packaging

1 BLISTER PACK in 1 CARTON (69842-973-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
1 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

69842-973-20 1 BLISTER PACK in 1 CARTON (69842-973-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 69842-973-30 1 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

fexofenadine hydrochloride (60 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "136bd5d9-aea8-4a79-985d-35ddd01de47b", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["45d3ad69-a80a-4f91-9c9b-8b19a30144a3"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-973-20)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-973-20", "marketing_start_date": "20200827"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-973-30)  / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-973-30", "marketing_start_date": "20200827"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "69842-973_136bd5d9-aea8-4a79-985d-35ddd01de47b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "69842-973", "generic_name": "FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090818", "marketing_category": "ANDA", "marketing_start_date": "20200827", "listing_expiration_date": "20261231"}