ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 750 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-078
Product ID 65862-078_9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Marketing Start 2007-04-26
Marketing End 2027-01-31

Pharmacologic Class

Classes
cytochrome p450 1a2 inhibitors [moa] fluoroquinolone antibacterial [epc] fluoroquinolones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862078
Hyphenated Format 65862-078

Supplemental Identifiers

RxCUI
197511 197512 309309
UPC
0365862076304 0365862078506 0365862077301
UNII
4BA73M5E37

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 ciprofloxacin (source: ndc)
Generic Name ciprofloxacin hydrochloride (source: ndc)
Application Number ANDA077859 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 50 TABLET, FILM COATED in 1 BOTTLE (65862-078-50)
source: ndc

Packages (1)

65862-078-50 50 TABLET, FILM COATED in 1 BOTTLE (65862-078-50)

Ingredients (1)

ciprofloxacin hydrochloride (750 mg/1)

Linked Drug Pages (1)

Ciprofloxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10", "openfda": {"upc": ["0365862076304", "0365862078506", "0365862077301"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["2b3b6a9f-259c-4736-b88f-f49d1eb64286"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (65862-078-50)", "package_ndc": "65862-078-50", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}], "brand_name": "Ciprofloxacin", "product_id": "65862-078_9e7eb1ac-3e09-4b4c-8ce1-ab16c3102a10", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "65862-078", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20070426"}