levofloxacin
Generic: levofloxacin
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
levofloxacin
Generic Name
levofloxacin
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
levofloxacin 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-1860
Product ID
68071-1860_2abbc9fa-1dc6-cbbc-e063-6294a90aa735
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202801
Listing Expiration
2026-12-31
Marketing Start
2015-01-09
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680711860
Hyphenated Format
68071-1860
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
levofloxacin (source: ndc)
Generic Name
levofloxacin (source: ndc)
Application Number
ANDA202801 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 20 TABLET, FILM COATED in 1 BOTTLE (68071-1860-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2abbc9fa-1dc6-cbbc-e063-6294a90aa735", "openfda": {"nui": ["N0000193223", "M0372253"], "upc": ["0368071186024"], "unii": ["6GNT3Y5LMF"], "rxcui": ["311296"], "spl_set_id": ["8423b021-e09c-4f1c-e053-2991aa0afef6"], "pharm_class_cs": ["Fluoroquinolones [CS]"], "pharm_class_epc": ["Fluoroquinolone Antibacterial [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-1860-2)", "package_ndc": "68071-1860-2", "marketing_start_date": "20190315"}], "brand_name": "Levofloxacin", "product_id": "68071-1860_2abbc9fa-1dc6-cbbc-e063-6294a90aa735", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68071-1860", "generic_name": "Levofloxacin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levofloxacin", "active_ingredients": [{"name": "LEVOFLOXACIN", "strength": "750 mg/1"}], "application_number": "ANDA202801", "marketing_category": "ANDA", "marketing_start_date": "20150109", "listing_expiration_date": "20261231"}