Package 69729-139-14

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69729-139-14
Digits Only 6972913914
Product NDC 69729-139
Product ID 69729-139_18ab8b3c-80f1-72ea-e063-6394a90ac0d1
Description

14 TABLET in 1 BOTTLE (69729-139-14)

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cetirizine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "18ab8b3c-80f1-72ea-e063-6394a90ac0d1", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["b452bca6-2c51-d0a1-e053-2995a90aff67"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (69729-139-14)", "package_ndc": "69729-139-14", "marketing_start_date": "20200701"}], "brand_name": "Cetirizine hydrochloride", "product_id": "69729-139_18ab8b3c-80f1-72ea-e063-6394a90ac0d1", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69729-139", "generic_name": "Cetirizine hydrochloride", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}