Package 68083-210-01
Brand: moxifloxacin ophthalmic solution
Generic: moxifloxacin ophthalmicPackage Facts
Identity
Package NDC
68083-210-01
Digits Only
6808321001
Product NDC
68083-210
Description
1 BOTTLE, PLASTIC in 1 CARTON (68083-210-01) / 3 mL in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
moxifloxacin ophthalmic solution
Generic
moxifloxacin ophthalmic
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1762525e-0af9-445f-ab67-00bfa954dc7d", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["95773bca-0791-4bfe-955a-4d2fa4561e01"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68083-210-01) / 3 mL in 1 BOTTLE, PLASTIC", "package_ndc": "68083-210-01", "marketing_start_date": "20200330"}], "brand_name": "Moxifloxacin Ophthalmic Solution", "product_id": "68083-210_1762525e-0af9-445f-ab67-00bfa954dc7d", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "68083-210", "generic_name": "Moxifloxacin Ophthalmic", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Ophthalmic Solution", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA208778", "marketing_category": "ANDA", "marketing_start_date": "20200330", "listing_expiration_date": "20261231"}