Package 72789-037-10

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-037-10
Digits Only 7278903710
Product NDC 72789-037
Product ID 72789-037_4af330aa-a2fd-3417-e063-6294a90adb69
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-037-10)

Marketing

Marketing Status
Marketed Since 2020-02-17
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af330aa-a2fd-3417-e063-6294a90adb69", "openfda": {"upc": ["0372789037103"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["1a98b20d-c4a1-4184-8387-a4866d1d62bf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-037-10)", "package_ndc": "72789-037-10", "marketing_start_date": "20200217"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "72789-037_4af330aa-a2fd-3417-e063-6294a90adb69", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-037", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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": "20271231"}