Package 0832-1410-03

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0832-1410-03
Digits Only 0832141003
Product NDC 0832-1410
Description

1 BOTTLE, PLASTIC in 1 CARTON (0832-1410-03) / 3 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2021-02-10
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "b740604e-1d7a-4382-90ca-26b0186f7a93", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["5a5d72e2-aa39-4ead-af72-d3cabe72a5b7"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0832-1410-03)  / 3 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0832-1410-03", "marketing_start_date": "20210210"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "0832-1410_b740604e-1d7a-4382-90ca-26b0186f7a93", "dosage_form": "SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "0832-1410", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA212616", "marketing_category": "ANDA", "marketing_start_date": "20210210", "listing_expiration_date": "20261231"}