Package 57237-156-30

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57237-156-30
Digits Only 5723715630
Product NDC 57237-156
Product ID 57237-156_20ac52fe-93eb-47c8-8bab-37f745f795fb
Description

30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)

Marketing

Marketing Status
Marketed Since 2014-03-04
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Moxifloxacin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20ac52fe-93eb-47c8-8bab-37f745f795fb", "openfda": {"upc": ["0357237156308"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["f34c08e6-fe74-4de3-9e36-a82c3c1c183b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)", "package_ndc": "57237-156-30", "marketing_start_date": "20140304"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "57237-156_20ac52fe-93eb-47c8-8bab-37f745f795fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "57237-156", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA202632", "marketing_category": "ANDA", "marketing_start_date": "20140304", "listing_expiration_date": "20261231"}