Package 68196-107-15

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68196-107-15
Digits Only 6819610715
Product NDC 68196-107
Description

1 BOTTLE in 1 CARTON (68196-107-15) / 150 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-05-09
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "573483c1-14c7-7ff1-a6ee-2d01a988333a", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1c1f43c4-7128-37c4-83fe-7eefac3fd477"], "manufacturer_name": ["Sam's West Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68196-107-15)  / 150 TABLET in 1 BOTTLE", "package_ndc": "68196-107-15", "marketing_start_date": "20170509"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (68196-107-50)", "package_ndc": "68196-107-50", "marketing_start_date": "20230401"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "68196-107_573483c1-14c7-7ff1-a6ee-2d01a988333a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68196-107", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Sam's West Inc.", "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": "20170509", "listing_expiration_date": "20261231"}