Package 47335-343-88

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-343-88
Digits Only 4733534388
Product NDC 47335-343
Product ID 47335-343_2ffbb45f-ed2b-4f1a-bc4c-1e8c1ddcbfd3
Description

100 TABLET, CHEWABLE in 1 BOTTLE (47335-343-88)

Marketing

Marketing Status
Marketed Since 2011-09-09
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": "2ffbb45f-ed2b-4f1a-bc4c-1e8c1ddcbfd3", "openfda": {"upc": ["0347335344837", "0347335343830"], "unii": ["64O047KTOA"], "rxcui": ["1014643", "1014674"], "spl_set_id": ["a4758152-97dd-4a27-b4d9-11178654b93e"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (47335-343-83)", "package_ndc": "47335-343-83", "marketing_start_date": "20110909"}, {"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (47335-343-88)", "package_ndc": "47335-343-88", "marketing_start_date": "20110909"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "47335-343_2ffbb45f-ed2b-4f1a-bc4c-1e8c1ddcbfd3", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "47335-343", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090142", "marketing_category": "ANDA", "marketing_start_date": "20110909", "listing_expiration_date": "20261231"}