Package 71335-2815-1

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2815-1
Digits Only 7133528151
Product NDC 71335-2815
Product ID 71335-2815_6ac508d3-c5c6-49b1-ab21-56896601f8ad
Description

7 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1)

Marketing

Marketing Status
Marketed Since 2025-10-15
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": "6ac508d3-c5c6-49b1-ab21-56896601f8ad", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["ac8a81b9-2fed-412a-8c83-db8dee1061f6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1)", "package_ndc": "71335-2815-1", "marketing_start_date": "20251015"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-2815-2)", "package_ndc": "71335-2815-2", "marketing_start_date": "20251015"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "71335-2815_6ac508d3-c5c6-49b1-ab21-56896601f8ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "71335-2815", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20261231"}