Package 68210-4159-1

Brand: allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68210-4159-1
Digits Only 6821041591
Product NDC 68210-4159
Description

1 BLISTER PACK in 1 CARTON (68210-4159-1) / 14 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-05-26
Brand allergy relief
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4949097a-aedb-eb3c-e063-6294a90a1192", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["e0e5f482-0282-410c-8c40-0a33ca4ea23a"], "manufacturer_name": ["Prodose, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68210-4159-1)  / 14 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68210-4159-1", "marketing_start_date": "20210526"}], "brand_name": "Allergy Relief", "product_id": "68210-4159_4949097a-aedb-eb3c-e063-6294a90a1192", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68210-4159", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Prodose, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077829", "marketing_category": "ANDA", "marketing_start_date": "20210428", "listing_expiration_date": "20271231"}