fexofenadine hydrochloride
Generic: fexofenadine hydrochloride
Labeler: walgreens companyDrug Facts
Product Profile
Brand Name
fexofenadine hydrochloride
Generic Name
fexofenadine hydrochloride
Labeler
walgreens company
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0783
Product ID
0363-0783_99bc952b-03e9-cb28-9669-ce7dfef79b0d
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076502
Listing Expiration
2026-12-31
Marketing Start
2020-12-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630783
Hyphenated Format
0363-0783
Supplemental Identifiers
UNII
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 (source: ndc)
Generic Name
fexofenadine hydrochloride (source: ndc)
Application Number
ANDA076502 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (0363-0783-24) / 6 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99bc952b-03e9-cb28-9669-ce7dfef79b0d", "openfda": {"unii": ["2S068B75ZU"], "spl_set_id": ["b961985e-0c18-b36f-d82e-32ff2d46fada"], "manufacturer_name": ["Walgreens Company"]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-0783-24) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0783-24", "marketing_start_date": "20201214"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "0363-0783_99bc952b-03e9-cb28-9669-ce7dfef79b0d", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-0783", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20201214", "listing_expiration_date": "20261231"}