fexofenadine hydrochloride and pseudoephedrine hydrochloride

Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloride

Labeler: walgreens 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 walgreens company
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
Walgreens Company

Identifiers & Regulatory

Product NDC 0363-0044
Product ID 0363-0044_5bd27db7-8135-aba8-7abd-8096cbc5b212
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 03630044
Hyphenated Format 0363-0044

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 (0363-0044-20) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 6 BLISTER PACK in 1 CARTON (0363-0044-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5bd27db7-8135-aba8-7abd-8096cbc5b212", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["db671b6e-7233-8872-0227-6da62d6b6507"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-0044-20)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0044-20", "marketing_start_date": "20230331"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0363-0044-30)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0044-30", "marketing_start_date": "20230331"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "0363-0044_5bd27db7-8135-aba8-7abd-8096cbc5b212", "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": "0363-0044", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Walgreens 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"}