childrens fexofenadine hydrochloride allergy

Generic: fexofenadine hydrochloride

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

Drug Facts

Product Profile

Brand Name childrens fexofenadine hydrochloride allergy
Generic Name fexofenadine hydrochloride
Labeler walgreens company
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 30 mg/5mL

Manufacturer
Walgreens Company

Identifiers & Regulatory

Product NDC 0363-2141
Product ID 0363-2141_374f99cb-1562-7532-e063-6394a90a95b4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA208123
Listing Expiration 2026-12-31
Marketing Start 2024-12-06

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03632141
Hyphenated Format 0363-2141

Supplemental Identifiers

RxCUI
997491
UNII
2S068B75ZU

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 childrens fexofenadine hydrochloride allergy (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA208123 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-2141-01) / 240 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-2141-08) / 120 mL in 1 BOTTLE
source: ndc

Packages (2)

0363-2141-01 1 BOTTLE in 1 CARTON (0363-2141-01) / 240 mL in 1 BOTTLE 0363-2141-08 1 BOTTLE in 1 CARTON (0363-2141-08) / 120 mL in 1 BOTTLE

Ingredients (1)

fexofenadine hydrochloride (30 mg/5mL)

Linked Drug Pages (1)

Childrens Fexofenadine Hydrochloride Allergy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "374f99cb-1562-7532-e063-6394a90a95b4", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997491"], "spl_set_id": ["374f9271-b65b-69a9-e063-6394a90af36a"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-2141-01)  / 240 mL in 1 BOTTLE", "package_ndc": "0363-2141-01", "marketing_start_date": "20241206"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-2141-08)  / 120 mL in 1 BOTTLE", "package_ndc": "0363-2141-08", "marketing_start_date": "20241206"}], "brand_name": "Childrens Fexofenadine Hydrochloride Allergy", "product_id": "0363-2141_374f99cb-1562-7532-e063-6394a90a95b4", "dosage_form": "SUSPENSION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-2141", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Fexofenadine Hydrochloride", "brand_name_suffix": "Allergy", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "30 mg/5mL"}], "application_number": "ANDA208123", "marketing_category": "ANDA", "marketing_start_date": "20241206", "listing_expiration_date": "20261231"}