Package 0781-7135-93

Brand: moxifloxacin ophthalmic solution

Generic: moxifloxacin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-7135-93
Digits Only 0781713593
Product NDC 0781-7135
Product ID 0781-7135_fe09f635-c4f0-4698-8468-d226257b6d58
Description

1 BOTTLE, PLASTIC in 1 CARTON (0781-7135-93) / 3 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2017-06-30
Brand moxifloxacin ophthalmic solution
Generic moxifloxacin hydrochloride
Sample Package No

Linked Drug Pages (1)

Moxifloxacin Ophthalmic Solution ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "fe09f635-c4f0-4698-8468-d226257b6d58", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["fc88791b-24da-48a4-85f5-93a8af3d0b51"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0781-7135-93)  / 3 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0781-7135-93", "marketing_start_date": "20170630"}], "brand_name": "Moxifloxacin Ophthalmic Solution", "product_id": "0781-7135_fe09f635-c4f0-4698-8468-d226257b6d58", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "0781-7135", "generic_name": "moxifloxacin hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Ophthalmic Solution", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "NDA021598", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20030507", "listing_expiration_date": "20261231"}