fexofenadine hydrochloride and pseudoephedrine hydrochloride

Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloride

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Generic Name fexofenadine hydrochloride and pseudoephedrine hydrochloride
Labeler kroger company
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 30142-097
Product ID 30142-097_1e577802-6930-b223-0c62-b4e1ad0a6048
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215434
Listing Expiration 2026-12-31
Marketing Start 2022-03-31

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 30142097
Hyphenated Format 30142-097

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 ANDA215434 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 CARTON (30142-097-20) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

30142-097-20 4 BLISTER PACK in 1 CARTON (30142-097-20) / 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 Hydrochloride and Pseudoephedrine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1e577802-6930-b223-0c62-b4e1ad0a6048", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["ac67476a-2888-53c4-0a10-7f73ac2580c5"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (30142-097-20)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "30142-097-20", "marketing_start_date": "20230601"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "30142-097_1e577802-6930-b223-0c62-b4e1ad0a6048", "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": "30142-097", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Kroger Company", "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": "ANDA215434", "marketing_category": "ANDA", "marketing_start_date": "20220331", "listing_expiration_date": "20261231"}