moxifloxacin hydrochloride
Generic: moxifloxacin hydrochloride
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
moxifloxacin hydrochloride
Generic Name
moxifloxacin hydrochloride
Labeler
asclemed usa, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
moxifloxacin hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-331
Product ID
76420-331_331b69c5-5ad7-a90a-e063-6394a90acfd6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212616
Listing Expiration
2026-12-31
Marketing Start
2021-02-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420331
Hyphenated Format
76420-331
Supplemental Identifiers
RxCUI
UNII
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 hydrochloride (source: ndc)
Generic Name
moxifloxacin hydrochloride (source: ndc)
Application Number
ANDA212616 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (76420-331-03) / 3 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "331b69c5-5ad7-a90a-e063-6394a90acfd6", "openfda": {"unii": ["C53598599T"], "rxcui": ["403818"], "spl_set_id": ["8f92f110-32d6-4d0c-a415-7a9a4cafb9b8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (76420-331-03) / 3 mL in 1 BOTTLE, PLASTIC", "package_ndc": "76420-331-03", "marketing_start_date": "20250419"}], "brand_name": "Moxifloxacin Hydrochloride", "product_id": "76420-331_331b69c5-5ad7-a90a-e063-6394a90acfd6", "dosage_form": "SOLUTION", "pharm_class": ["Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "76420-331", "generic_name": "Moxifloxacin Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA212616", "marketing_category": "ANDA", "marketing_start_date": "20210210", "listing_expiration_date": "20261231"}