moxifloxacin

Generic: moxifloxacin

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin
Generic Name moxifloxacin
Labeler redpharm drug
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

moxifloxacin hydrochloride monohydrate 5 mg/mL

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2129
Product ID 67296-2129_4698d4e7-2e86-6fbf-e063-6294a90a0d1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202867
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 672962129
Hyphenated Format 67296-2129

Supplemental Identifiers

RxCUI
403818
UPC
0368180422013
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 ANDA202867 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (67296-2129-3) / 3 mL in 1 BOTTLE
source: ndc

Packages (1)

67296-2129-3 1 BOTTLE in 1 CARTON (67296-2129-3) / 3 mL in 1 BOTTLE

Ingredients (1)

moxifloxacin hydrochloride monohydrate (5 mg/mL)

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "4698d4e7-2e86-6fbf-e063-6294a90a0d1e", "openfda": {"upc": ["0368180422013"], "unii": ["B8956S8609"], "rxcui": ["403818"], "spl_set_id": ["301eef74-16db-14aa-e063-6294a90ac8ff"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (67296-2129-3)  / 3 mL in 1 BOTTLE", "package_ndc": "67296-2129-3", "marketing_start_date": "20170701"}], "brand_name": "Moxifloxacin", "product_id": "67296-2129_4698d4e7-2e86-6fbf-e063-6294a90a0d1e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "67296-2129", "generic_name": "Moxifloxacin", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "5 mg/mL"}], "application_number": "ANDA202867", "marketing_category": "ANDA", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}