Package 49483-682-01

Brand: cetirizine hydrochloride

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49483-682-01
Digits Only 4948368201
Product NDC 49483-682
Description

100 TABLET in 1 BOTTLE (49483-682-01)

Marketing

Marketing Status
Marketed Since 2022-05-30
Brand cetirizine hydrochloride
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dfbdaf6a-c5e8-c5f9-e053-2995a90ae2c6", "openfda": {"upc": ["0349483682014"], "unii": ["64O047KTOA"], "rxcui": ["1014676"], "spl_set_id": ["dfbddafb-9455-5805-e053-2a95a90ad0d9"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49483-682-01)", "package_ndc": "49483-682-01", "marketing_start_date": "20220530"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "49483-682_dfbdaf6a-c5e8-c5f9-e053-2995a90ae2c6", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "49483-682", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078933", "marketing_category": "ANDA", "marketing_start_date": "20220530", "listing_expiration_date": "20261231"}