Package 55681-302-03

Brand: cetirizine hydrochloride 10 mg

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55681-302-03
Digits Only 5568130203
Product NDC 55681-302
Product ID 55681-302_0e12b3c6-357a-b0dc-e063-6394a90a8ea4
Description

300 TABLET in 1 BOTTLE (55681-302-03)

Marketing

Marketing Status
Marketed Since 2022-03-02
Brand cetirizine hydrochloride 10 mg
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

CETIRIZINE HYDROCHLORIDE 10 MG ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e12b3c6-357a-b0dc-e063-6394a90a8ea4", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["d9437d88-da59-5567-e053-2995a90a362b"], "manufacturer_name": ["TWIN MED, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-302-03)", "package_ndc": "55681-302-03", "marketing_start_date": "20220302"}], "brand_name": "CETIRIZINE HYDROCHLORIDE 10 MG", "product_id": "55681-302_0e12b3c6-357a-b0dc-e063-6394a90a8ea4", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55681-302", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "TWIN MED, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CETIRIZINE HYDROCHLORIDE", "brand_name_suffix": "10 MG", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20261231"}