Package 70010-183-03

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 70010-183-03
Digits Only 7001018303
Product NDC 70010-183
Product ID 70010-183_451e21a2-6057-7a94-e063-6294a90a9f87
Description

30 TABLET in 1 BOTTLE (70010-183-03)

Marketing

Marketing Status
Marketed Since 2023-04-25
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Fexofenadine HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "451e21a2-6057-7a94-e063-6294a90a9f87", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["fa30c8ce-ad9d-b6fe-e053-6294a90a2443"], "manufacturer_name": ["GRANULES PHARMACEUTICALS INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70010-183-03)", "package_ndc": "70010-183-03", "marketing_start_date": "20230425"}], "brand_name": "Fexofenadine HCL", "product_id": "70010-183_451e21a2-6057-7a94-e063-6294a90a9f87", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70010-183", "generic_name": "Fexofenadine HCL", "labeler_name": "GRANULES PHARMACEUTICALS INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20230425", "listing_expiration_date": "20261231"}