Package 82667-700-03

Brand: vigamox

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82667-700-03
Digits Only 8266770003
Product NDC 82667-700
Product ID 82667-700_48fbfef1-1e3b-4558-e063-6394a90a2454
Description

1 BOTTLE in 1 CARTON (82667-700-03) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-07-01
Brand vigamox
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

VIGAMOX ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "48fbfef1-1e3b-4558-e063-6394a90a2454", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818", "404473"], "spl_set_id": ["12053b08-7e66-c6f3-e063-6394a90a9cd9"], "manufacturer_name": ["Harrow Eye, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82667-700-03)  / 3 mL in 1 BOTTLE", "package_ndc": "82667-700-03", "marketing_start_date": "20240701"}], "brand_name": "VIGAMOX", "product_id": "82667-700_48fbfef1-1e3b-4558-e063-6394a90a2454", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "82667-700", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Harrow Eye, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIGAMOX", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "NDA021598", "marketing_category": "NDA", "marketing_start_date": "20240701", "listing_expiration_date": "20271231"}