Package 72789-080-10

Brand: moxifloxacin hydrochloride tablets, 400 mg

Generic: moxifloxacin hydrochloride tablets, 400 mg
NDC Package

Package Facts

Identity

Package NDC 72789-080-10
Digits Only 7278908010
Product NDC 72789-080
Product ID 72789-080_40319333-cf76-1664-e063-6294a90ae7e8
Description

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10)

Marketing

Marketing Status
Marketed Since 2020-04-10
Brand moxifloxacin hydrochloride tablets, 400 mg
Generic moxifloxacin hydrochloride tablets, 400 mg
Sample Package No

Linked Drug Pages (1)

Moxifloxacin Hydrochloride Tablets, 400 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40319333-cf76-1664-e063-6294a90ae7e8", "openfda": {"upc": ["0372789080109"], "unii": ["B8956S8609"], "rxcui": ["311787"], "spl_set_id": ["5c2a9116-d6e4-429e-88bb-bb6bfedac2f0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10)", "package_ndc": "72789-080-10", "marketing_start_date": "20200410"}], "brand_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "product_id": "72789-080_40319333-cf76-1664-e063-6294a90ae7e8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72789-080", "generic_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride Tablets, 400 mg", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "400 mg/1"}], "application_number": "ANDA208682", "marketing_category": "ANDA", "marketing_start_date": "20180721", "listing_expiration_date": "20261231"}