Package 63868-025-30

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63868-025-30
Digits Only 6386802530
Product NDC 63868-025
Product ID 63868-025_b1eeea1a-04f8-d205-fe4a-13699ea6bb47
Description

1 BOTTLE in 1 CARTON (63868-025-30) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2014-04-01
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": "b1eeea1a-04f8-d205-fe4a-13699ea6bb47", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["8a1de8a1-808a-bc08-6c74-957d6f388eab"], "manufacturer_name": ["Chain Drug Marketing Associate"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-025-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "63868-025-30", "marketing_start_date": "20140401"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "63868-025_b1eeea1a-04f8-d205-fe4a-13699ea6bb47", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63868-025", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Chain Drug Marketing Associate", "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": "20140401", "listing_expiration_date": "20261231"}