ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: carlsbad technology, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler carlsbad technology, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 750 mg/1

Manufacturer
Carlsbad Technology, Inc.

Identifiers & Regulatory

Product NDC 61442-224
Product ID 61442-224_2d6a2060-1f59-696d-e063-6394a90a2796
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076126
Listing Expiration 2026-12-31
Marketing Start 2009-10-10

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 61442224
Hyphenated Format 61442-224

Supplemental Identifiers

RxCUI
197511 197512 309309
UPC
0361442222017 0361442223014 0361442224509
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 ANDA076126 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)
  • 50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)
source: ndc

Packages (2)

61442-224-04 400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04) 61442-224-50 50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)

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": "2d6a2060-1f59-696d-e063-6394a90a2796", "openfda": {"upc": ["0361442222017", "0361442223014", "0361442224509"], "unii": ["4BA73M5E37"], "rxcui": ["197511", "197512", "309309"], "spl_set_id": ["37527eca-115e-4582-88cd-bba851ac6069"], "manufacturer_name": ["Carlsbad Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)", "package_ndc": "61442-224-04", "marketing_start_date": "20091010"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (61442-224-50)", "package_ndc": "61442-224-50", "marketing_start_date": "20091010"}], "brand_name": "Ciprofloxacin", "product_id": "61442-224_2d6a2060-1f59-696d-e063-6394a90a2796", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "61442-224", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "Carlsbad Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA076126", "marketing_category": "ANDA", "marketing_start_date": "20091010", "listing_expiration_date": "20261231"}