ciprofloxacin

Generic: ciprofloxacin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ciprofloxacin hydrochloride 250 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2146
Product ID 50090-2146_ef857039-e741-4c82-bb4d-01fb8fd3f15e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077859
Listing Expiration 2026-12-31
Marketing Start 2007-04-26

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 500902146
Hyphenated Format 50090-2146

Supplemental Identifiers

RxCUI
197511
UNII
4BA73M5E37

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
  • 250 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE (50090-2146-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-2146-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-2146-2)
  • 3 TABLET, FILM COATED in 1 BOTTLE (50090-2146-3)
source: ndc

Packages (4)

50090-2146-0 6 TABLET, FILM COATED in 1 BOTTLE (50090-2146-0) 50090-2146-1 14 TABLET, FILM COATED in 1 BOTTLE (50090-2146-1) 50090-2146-2 10 TABLET, FILM COATED in 1 BOTTLE (50090-2146-2) 50090-2146-3 3 TABLET, FILM COATED in 1 BOTTLE (50090-2146-3)

Ingredients (1)

ciprofloxacin hydrochloride (250 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": "ef857039-e741-4c82-bb4d-01fb8fd3f15e", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["197511"], "spl_set_id": ["4dd69fb7-802a-4278-a730-c722a3ca3521"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-2146-0)", "package_ndc": "50090-2146-0", "marketing_start_date": "20151020"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-2146-1)", "package_ndc": "50090-2146-1", "marketing_start_date": "20151020"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-2146-2)", "package_ndc": "50090-2146-2", "marketing_start_date": "20151020"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-2146-3)", "package_ndc": "50090-2146-3", "marketing_start_date": "20190813"}], "brand_name": "Ciprofloxacin", "product_id": "50090-2146_ef857039-e741-4c82-bb4d-01fb8fd3f15e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-2146", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077859", "marketing_category": "ANDA", "marketing_start_date": "20070426", "listing_expiration_date": "20261231"}