Package 68180-421-01

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 68180-421-01
Digits Only 6818042101
Product NDC 68180-421
Product ID 68180-421_29272b83-77cf-4cd1-9aed-b80d0cc6edb5
Description

3 mL in 1 BOTTLE (68180-421-01)

Marketing

Marketing Status
Marketed Since 2020-02-13
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": "29272b83-77cf-4cd1-9aed-b80d0cc6edb5", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["d66f080b-da56-4473-8785-920d9700f72d"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 mL in 1 BOTTLE (68180-421-01)", "package_ndc": "68180-421-01", "marketing_start_date": "20200213"}], "brand_name": "MOXIFLOXACIN", "product_id": "68180-421_29272b83-77cf-4cd1-9aed-b80d0cc6edb5", "dosage_form": "SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "68180-421", "generic_name": "MOXIFLOXACIN", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOXIFLOXACIN", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA204079", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20261231"}