ciprofloxacin

Generic: ciprofloxacin

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

Drug Facts

Product Profile

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

ciprofloxacin hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1648
Product ID 50090-1648_5f4acec7-3462-49b9-962c-931fedc0f520
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076639
Listing Expiration 2026-12-31
Marketing Start 2004-09-10

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 500901648
Hyphenated Format 50090-1648

Supplemental Identifiers

RxCUI
309309
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 (source: ndc)
Application Number ANDA076639 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-1648-0)
  • 14 TABLET in 1 BOTTLE (50090-1648-1)
  • 6 TABLET in 1 BOTTLE (50090-1648-3)
  • 28 TABLET in 1 BOTTLE (50090-1648-4)
  • 10 TABLET in 1 BOTTLE (50090-1648-5)
  • 30 TABLET in 1 BOTTLE (50090-1648-7)
  • 1 TABLET in 1 BOTTLE (50090-1648-8)
source: ndc

Packages (7)

50090-1648-0 20 TABLET in 1 BOTTLE (50090-1648-0) 50090-1648-1 14 TABLET in 1 BOTTLE (50090-1648-1) 50090-1648-3 6 TABLET in 1 BOTTLE (50090-1648-3) 50090-1648-4 28 TABLET in 1 BOTTLE (50090-1648-4) 50090-1648-5 10 TABLET in 1 BOTTLE (50090-1648-5) 50090-1648-7 30 TABLET in 1 BOTTLE (50090-1648-7) 50090-1648-8 1 TABLET in 1 BOTTLE (50090-1648-8)

Ingredients (1)

ciprofloxacin hydrochloride (500 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": "5f4acec7-3462-49b9-962c-931fedc0f520", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["c12b316f-811c-48b6-a320-d314991aa74f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-1648-0)", "package_ndc": "50090-1648-0", "marketing_start_date": "20150119"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-1648-1)", "package_ndc": "50090-1648-1", "marketing_start_date": "20150119"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (50090-1648-3)", "package_ndc": "50090-1648-3", "marketing_start_date": "20150119"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-1648-4)", "package_ndc": "50090-1648-4", "marketing_start_date": "20150119"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-1648-5)", "package_ndc": "50090-1648-5", "marketing_start_date": "20150119"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1648-7)", "package_ndc": "50090-1648-7", "marketing_start_date": "20150119"}, {"sample": false, "description": "1 TABLET in 1 BOTTLE (50090-1648-8)", "package_ndc": "50090-1648-8", "marketing_start_date": "20180522"}], "brand_name": "ciprofloxacin", "product_id": "50090-1648_5f4acec7-3462-49b9-962c-931fedc0f520", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "50090-1648", "generic_name": "ciprofloxacin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076639", "marketing_category": "ANDA", "marketing_start_date": "20040910", "listing_expiration_date": "20261231"}