fexofenadine hydrochloride

Generic: fexofenadine hydrochloride

Labeler: strategic sourcing services, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fexofenadine hydrochloride
Generic Name fexofenadine hydrochloride
Labeler strategic sourcing services, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Strategic Sourcing Services, LLC

Identifiers & Regulatory

Product NDC 70677-1009
Product ID 70677-1009_1982b8ab-b306-c1f8-0490-943207d2b606
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076502
Listing Expiration 2026-12-31
Marketing Start 2019-09-09

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 706771009
Hyphenated Format 70677-1009

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (70677-1009-1) / 5 TABLET in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (70677-1009-2) / 30 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (70677-1009-3) / 70 TABLET in 1 BOTTLE
source: ndc

Packages (3)

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1982b8ab-b306-c1f8-0490-943207d2b606", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["de438313-9790-b4ea-2d28-7a19836cf5e2"], "manufacturer_name": ["Strategic Sourcing Services, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70677-1009-1)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "70677-1009-1", "marketing_start_date": "20230505"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70677-1009-2)  / 30 TABLET in 1 BOTTLE", "package_ndc": "70677-1009-2", "marketing_start_date": "20230505"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (70677-1009-3)  / 70 TABLET in 1 BOTTLE", "package_ndc": "70677-1009-3", "marketing_start_date": "20230505"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "70677-1009_1982b8ab-b306-c1f8-0490-943207d2b606", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70677-1009", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Strategic Sourcing Services, LLC", "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": "20190909", "listing_expiration_date": "20261231"}