Package 16714-643-01

Brand: moxifloxacin

Generic: moxifloxacin
NDC Package

Package Facts

Identity

Package NDC 16714-643-01
Digits Only 1671464301
Product NDC 16714-643
Product ID 16714-643_c11c970c-ffa6-4661-b515-708bae4eddd6
Description

1 BOTTLE in 1 CARTON (16714-643-01) / 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": "c11c970c-ffa6-4661-b515-708bae4eddd6", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["cdc0b0eb-5f56-45c7-b9fd-364752a95ff1"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (16714-643-01)  / 3 mL in 1 BOTTLE", "package_ndc": "16714-643-01", "marketing_start_date": "20171004"}], "brand_name": "MOXIFLOXACIN", "product_id": "16714-643_c11c970c-ffa6-4661-b515-708bae4eddd6", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "16714-643", "generic_name": "MOXIFLOXACIN", "labeler_name": "NorthStar Rx LLC", "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"}