Package 70518-3738-0

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3738-0
Digits Only 7051837380
Product NDC 70518-3738
Product ID 70518-3738_3f63002b-3ecc-2ca5-e063-6294a90a7c33
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3738-0)

Marketing

Marketing Status
Marketed Since 2023-05-30
Brand moxifloxacin hydrochloride
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f63002b-3ecc-2ca5-e063-6294a90a7c33", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["bd0c0690-ba48-41c5-b76b-b1a53c36f424"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3738-0)", "package_ndc": "70518-3738-0", "marketing_start_date": "20230530"}], "brand_name": "MOXIFLOXACIN HYDROCHLORIDE", "product_id": "70518-3738_3f63002b-3ecc-2ca5-e063-6294a90a7c33", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70518-3738", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "REMEDYREPACK 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": "20230530", "listing_expiration_date": "20261231"}