Package 55910-111-30

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55910-111-30
Digits Only 5591011130
Product NDC 55910-111
Product ID 55910-111_70e933f5-e72a-663c-784c-2eb38e453301
Description

1 BOTTLE in 1 CARTON (55910-111-30) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-07-17
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": "70e933f5-e72a-663c-784c-2eb38e453301", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1b2a14a1-a5cc-4f5e-8127-57e9d913f50a"], "manufacturer_name": ["Dollar General"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-111-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "55910-111-30", "marketing_start_date": "20190717"}], "brand_name": "Fexofenadine hydrochloride", "product_id": "55910-111_70e933f5-e72a-663c-784c-2eb38e453301", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-111", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Dollar General", "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": "20190717", "listing_expiration_date": "20261231"}