Package 50268-576-13

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-576-13
Digits Only 5026857613
Product NDC 50268-576
Product ID 50268-576_47e7ca84-9c19-3d8e-e063-6294a90a8903
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)

Marketing

Marketing Status
Marketed Since 2016-07-22
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": "47e7ca84-9c19-3d8e-e063-6294a90a8903", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["371ca7b2-c62d-ef4b-3076-890b385bfff8"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)", "package_ndc": "50268-576-13", "marketing_start_date": "20160722"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "50268-576_47e7ca84-9c19-3d8e-e063-6294a90a8903", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50268-576", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "AvPAK", "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": "20160722", "listing_expiration_date": "20271231"}