Package 70069-081-01

Brand: moxifloxacin hydrochloride

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-081-01
Digits Only 7006908101
Product NDC 70069-081
Product ID 70069-081_1a4f432a-c2b2-46bc-88fc-7379c2bbd0a2
Description

1 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-11-25
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": ["OPHTHALMIC"], "spl_id": "1a4f432a-c2b2-46bc-88fc-7379c2bbd0a2", "openfda": {"upc": ["0370069081013"], "unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["f7c68d49-8c61-4bde-a880-4d78568e5aa0"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-081-01)  / 3 mL in 1 BOTTLE", "package_ndc": "70069-081-01", "marketing_start_date": "20241125"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "70069-081_1a4f432a-c2b2-46bc-88fc-7379c2bbd0a2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "70069-081", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA209698", "marketing_category": "ANDA", "marketing_start_date": "20241125", "listing_expiration_date": "20261231"}