Package 65862-840-03

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 65862-840-03
Digits Only 6586284003
Product NDC 65862-840
Product ID 65862-840_95a06b0b-fd23-4b1b-9813-105678b10b6c
Description

1 BOTTLE in 1 CARTON (65862-840-03) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-10-04
Brand moxifloxacin
Generic moxifloxacin
Sample Package No

Linked Drug Pages (1)

MOXIFLOXACIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "95a06b0b-fd23-4b1b-9813-105678b10b6c", "openfda": {"upc": ["0365862840035"], "unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["8877013d-9b49-40f7-a2c4-99bb519e104e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (65862-840-03)  / 3 mL in 1 BOTTLE", "package_ndc": "65862-840-03", "marketing_start_date": "20171004"}], "brand_name": "MOXIFLOXACIN", "product_id": "65862-840_95a06b0b-fd23-4b1b-9813-105678b10b6c", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "65862-840", "generic_name": "MOXIFLOXACIN", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA206242", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}