Package 68998-292-04

Brand: allergy relief

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68998-292-04
Digits Only 6899829204
Product NDC 68998-292
Description

1 BOTTLE, PLASTIC in 1 CARTON (68998-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2021-07-09
Brand allergy relief
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ea60b4c2-b62a-61cf-e053-2995a90a6f56", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c4f93336-cfd8-e023-e053-2995a90a9df0"], "manufacturer_name": ["MARC GLASSMAN, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68998-292-04)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "68998-292-04", "marketing_start_date": "20210709"}], "brand_name": "Allergy Relief", "product_id": "68998-292_ea60b4c2-b62a-61cf-e053-2995a90a6f56", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68998-292", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "MARC GLASSMAN, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20261231"}