moxifloxacin

Generic: moxifloxacin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin
Generic Name moxifloxacin
Labeler bryant ranch prepack
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

moxifloxacin hydrochloride monohydrate 5 mg/mL

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2107
Product ID 72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090080
Listing Expiration 2026-12-31
Marketing Start 2017-07-01

Pharmacologic Class

Classes
fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622107
Hyphenated Format 72162-2107

Supplemental Identifiers

RxCUI
403818
UNII
B8956S8609

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name moxifloxacin (source: ndc)
Generic Name moxifloxacin (source: ndc)
Application Number ANDA090080 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

Ingredients (1)

moxifloxacin hydrochloride monohydrate (5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68", "openfda": {"unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["1cc031d7-0766-41c0-b5b3-35119c850e23"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2)  / 3 mL in 1 BOTTLE, DROPPER", "package_ndc": "72162-2107-2", "marketing_start_date": "20170701"}], "brand_name": "Moxifloxacin", "product_id": "72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "72162-2107", "generic_name": "moxifloxacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA090080", "marketing_category": "ANDA", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}