Package 70677-1241-1

Brand: allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70677-1241-1
Digits Only 7067712411
Product NDC 70677-1241
Description

120 TABLET, FILM COATED in 1 BOTTLE (70677-1241-1)

Marketing

Marketing Status
Marketed Since 2024-01-24
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": "498adc5b-0e60-f64c-e063-6394a90a62ea", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["54509525-ad99-4165-a571-47ece058e292"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (70677-1241-1)", "package_ndc": "70677-1241-1", "marketing_start_date": "20240124"}], "brand_name": "Allergy Relief", "product_id": "70677-1241_498adc5b-0e60-f64c-e063-6394a90a62ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70677-1241", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Strategic Sourcing Services LLC", "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": "20240123", "listing_expiration_date": "20271231"}