Package 70518-4312-0

Brand: moxifloxacin hydrochloride tablets, 400 mg

Generic: moxifloxacin hydrochloride tablets, 400 mg
NDC Package

Package Facts

Identity

Package NDC 70518-4312-0
Digits Only 7051843120
Product NDC 70518-4312
Product ID 70518-4312_402db01e-845f-d529-e063-6394a90a16f9
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0)

Marketing

Marketing Status
Marketed Since 2025-03-18
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": "402db01e-845f-d529-e063-6394a90a16f9", "openfda": {"unii": ["B8956S8609"], "rxcui": ["311787"], "spl_set_id": ["bdb3f89a-01e7-411d-b071-48e87def0873"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0)", "package_ndc": "70518-4312-0", "marketing_start_date": "20250318"}], "brand_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "product_id": "70518-4312_402db01e-845f-d529-e063-6394a90a16f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-4312", "generic_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "labeler_name": "REMEDYREPACK 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": "20250318", "listing_expiration_date": "20261231"}