Package 67296-2129-3

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 67296-2129-3
Digits Only 6729621293
Product NDC 67296-2129
Product ID 67296-2129_4698d4e7-2e86-6fbf-e063-6294a90a0d1e
Description

1 BOTTLE in 1 CARTON (67296-2129-3) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-07-01
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": "4698d4e7-2e86-6fbf-e063-6294a90a0d1e", "openfda": {"upc": ["0368180422013"], "unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["301eef74-16db-14aa-e063-6294a90ac8ff"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (67296-2129-3)  / 3 mL in 1 BOTTLE", "package_ndc": "67296-2129-3", "marketing_start_date": "20170701"}], "brand_name": "Moxifloxacin", "product_id": "67296-2129_4698d4e7-2e86-6fbf-e063-6294a90a0d1e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67296-2129", "generic_name": "Moxifloxacin", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA202867", "marketing_category": "ANDA", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}