fexofenadine hcl and pseudoephedrine hci (59779-508)

Drug Facts

Product Profile

Brand Name fexofenadine hcl and pseudoephedrine hci

Generic Name fexofenadine hcl and pseudoephedrine hci

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 59779-508

Product ID 59779-508_aac03106-806f-bc8c-056c-bed65497dd54

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA076667

Listing Expiration 2026-12-31

Marketing Start 2014-11-19

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 59779508

Hyphenated Format 59779-508

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 hcl and pseudoephedrine hci (source: ndc)

Generic Name fexofenadine hcl and pseudoephedrine hci (source: ndc)

Application Number ANDA076667 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

60 mg/1
120 mg/1

source: ndc

Packaging

4 BLISTER PACK in 1 CARTON (59779-508-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
6 BLISTER PACK in 1 CARTON (59779-508-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

59779-508-14 4 BLISTER PACK in 1 CARTON (59779-508-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 59779-508-31 6 BLISTER PACK in 1 CARTON (59779-508-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

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

Linked Drug Pages (1)

Fexofenadine HCl and Pseudoephedrine HCI ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "aac03106-806f-bc8c-056c-bed65497dd54", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["3e295047-1a46-a0d8-2e3f-ec4086f5aedb"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (59779-508-14)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59779-508-14", "marketing_start_date": "20141119"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (59779-508-31)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59779-508-31", "marketing_start_date": "20141119"}], "brand_name": "Fexofenadine HCl and Pseudoephedrine HCI", "product_id": "59779-508_aac03106-806f-bc8c-056c-bed65497dd54", "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": "59779-508", "generic_name": "Fexofenadine HCl and Pseudoephedrine HCI", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCl and Pseudoephedrine HCI", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA076667", "marketing_category": "ANDA", "marketing_start_date": "20141119", "listing_expiration_date": "20261231"}