moxifloxacin

Generic: moxifloxacin

Labeler: dr. reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moxifloxacin
Generic Name moxifloxacin
Labeler dr. reddy's laboratories limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moxifloxacin hydrochloride 400 mg/1

Manufacturer
Dr. Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-112
Product ID 55111-112_b7966736-4865-d3ad-d218-886c8a286492
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076938
Listing Expiration 2026-12-31
Marketing Start 2014-03-05

Pharmacologic Class

Classes
quinolone antimicrobial [epc] quinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111112
Hyphenated Format 55111-112

Supplemental Identifiers

RxCUI
311787
UNII
C53598599T

Packaging Origin

Original Packager
true

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 ANDA076938 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)
  • 5 BLISTER PACK in 1 CARTON (55111-112-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)
source: ndc

Packages (4)

55111-112-01 100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01) 55111-112-05 500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05) 55111-112-30 30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30) 55111-112-66 5 BLISTER PACK in 1 CARTON (55111-112-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)

Ingredients (1)

moxifloxacin hydrochloride (400 mg/1)

Linked Drug Pages (1)

Moxifloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b7966736-4865-d3ad-d218-886c8a286492", "openfda": {"unii": ["C53598599T"], "rxcui": ["311787"], "spl_set_id": ["71b02da1-3175-1db8-192a-c0a8a6cd98a5"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)", "package_ndc": "55111-112-01", "marketing_start_date": "20140305"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)", "package_ndc": "55111-112-05", "marketing_start_date": "20140305"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)", "package_ndc": "55111-112-30", "marketing_start_date": "20140305"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (55111-112-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)", "package_ndc": "55111-112-66", "marketing_start_date": "20140305"}], "brand_name": "Moxifloxacin", "product_id": "55111-112_b7966736-4865-d3ad-d218-886c8a286492", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "55111-112", "generic_name": "Moxifloxacin", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE", "strength": "400 mg/1"}], "application_number": "ANDA076938", "marketing_category": "ANDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}