fexofenadine hydrochloride
Generic: fexofenadine hydrochloride
Labeler: dollar generalDrug Facts
Product Profile
Brand Name
fexofenadine hydrochloride
Generic Name
fexofenadine hydrochloride
Labeler
dollar general
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55910-111
Product ID
55910-111_70e933f5-e72a-663c-784c-2eb38e453301
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076502
Listing Expiration
2026-12-31
Marketing Start
2019-07-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910111
Hyphenated Format
55910-111
Supplemental Identifiers
RxCUI
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
- 180 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55910-111-30) / 30 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "70e933f5-e72a-663c-784c-2eb38e453301", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1b2a14a1-a5cc-4f5e-8127-57e9d913f50a"], "manufacturer_name": ["Dollar General"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-111-30) / 30 TABLET in 1 BOTTLE", "package_ndc": "55910-111-30", "marketing_start_date": "20190717"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "55910-111_70e933f5-e72a-663c-784c-2eb38e453301", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-111", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Dollar General", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20190717", "listing_expiration_date": "20261231"}