Package 43598-936-01

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43598-936-01
Digits Only 4359893601
Product NDC 43598-936
Product ID 43598-936_67592c0a-bfc4-9a83-0e70-b12b4b3cea84
Description

1 BOTTLE in 1 CARTON (43598-936-01) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-12-01
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": "67592c0a-bfc4-9a83-0e70-b12b4b3cea84", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["b0121213-eae1-8429-9986-3b3b26f35e47"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-936-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "43598-936-01", "marketing_start_date": "20201201"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "43598-936_67592c0a-bfc4-9a83-0e70-b12b4b3cea84", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "43598-936", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}