ciprofloxacin

Generic: ciprofloxacin

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ciprofloxacin
Generic Name ciprofloxacin
Labeler chartwell rx, llc
Dosage Form KIT
Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-392
Product ID 62135-392_459c475d-c9e2-ffa6-e063-6394a90add66
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200563
Listing Expiration 2026-12-31
Marketing Start 2014-03-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135392
Hyphenated Format 62135-392

Supplemental Identifiers

RxCUI
309308 309310
UPC
0362135393427 0362135392420

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 (source: ndc)
Application Number ANDA200563 (source: ndc)

Resolved Composition

Strengths
  • 5 %
  • 250 mg/5 ml
  • 10 %
  • 500 mg/5 ml
  • 250 mg
  • 5 ml
  • 500 mg
  • 100 ml
  • 5000 mg
  • 10000 mg
source: label
Packaging
  • 1 KIT in 1 KIT (62135-392-42) * 100 mL in 1 BOTTLE * 100 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "459c475d-c9e2-ffa6-e063-6394a90add66", "openfda": {"upc": ["0362135393427", "0362135392420"], "rxcui": ["309308", "309310"], "spl_set_id": ["905503ef-4277-44ca-aa4a-5a969a041e16"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (62135-392-42)  *  100 mL in 1 BOTTLE *  100 mL in 1 BOTTLE", "package_ndc": "62135-392-42", "marketing_start_date": "20230127"}], "brand_name": "ciprofloxacin", "product_id": "62135-392_459c475d-c9e2-ffa6-e063-6394a90add66", "dosage_form": "KIT", "product_ndc": "62135-392", "generic_name": "ciprofloxacin", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ciprofloxacin", "application_number": "ANDA200563", "marketing_category": "ANDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}