Package 72789-038-10

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-038-10
Digits Only 7278903810
Product NDC 72789-038
Product ID 72789-038_4af33f79-7627-6629-e063-6294a90ad764
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-038-10)

Marketing

Marketing Status
Marketed Since 2019-12-10
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": "4af33f79-7627-6629-e063-6294a90ad764", "openfda": {"upc": ["0372789038100"], "unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["18b77b31-baf3-416f-b3b7-a631c8e46d20"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-038-10)", "package_ndc": "72789-038-10", "marketing_start_date": "20191210"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "72789-038_4af33f79-7627-6629-e063-6294a90ad764", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-038", "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"}