Package 71309-091-01

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71309-091-01
Digits Only 7130909101
Product NDC 71309-091
Product ID 71309-091_f7f18cee-5649-13c4-e053-6294a90ad4a8
Description

100 TABLET in 1 BOTTLE (71309-091-01)

Marketing

Marketing Status
Marketed Since 2021-01-31
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fexofenadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f7f18cee-5649-13c4-e053-6294a90ad4a8", "openfda": {"upc": ["0371309091014"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d6120f56-ab28-2696-e053-2995a90adf47"], "manufacturer_name": ["Safrel Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71309-091-01)", "package_ndc": "71309-091-01", "marketing_start_date": "20210131"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "71309-091_f7f18cee-5649-13c4-e053-6294a90ad4a8", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71309-091", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Safrel Pharmaceuticals, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20210103", "listing_expiration_date": "20261231"}