ciprofloxacin

Orange BookUNIISPLATC J01MA02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerNuCare Pharmaceuticals,Inc.

CountryUS (United States)

ATC codeJ01MA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
6807142602
21 TABLET in 1 BOTTLE (68071-4260-2)
ndc11
6807142603
30 TABLET in 1 BOTTLE (68071-4260-3)
ndc11
6807142604
14 TABLET in 1 BOTTLE (68071-4260-4)
ndc11
6807142605
20 TABLET in 1 BOTTLE (68071-4260-5)
ndc11
6807142606
6 TABLET in 1 BOTTLE (68071-4260-6)
ndc11
6807142607
10 TABLET in 1 BOTTLE (68071-4260-7)
ndc11
6807142608
28 TABLET in 1 BOTTLE (68071-4260-8)
ndc11
6807142609
90 TABLET in 1 BOTTLE (68071-4260-9)

Annotations

UNII (FDA Substance ID)

4BA73M5E37

CIPROFLOXACIN HYDROCHLORIDE

RxCUI 81981

Orange Book

A076639

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4BA73M5E37",
    "rxcui": "81981",
    "inchikey": "ARPUHYJMCVWYCZ-UHFFFAOYSA-N",
    "display_name": "CIPROFLOXACIN HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a05035e1-f941-4f7c-9321-91dd50ab149b": {
      "match": "brand_token",
      "title": "CIPROFLOXACIN TABLET, COATED [BRYANT RANCH PREPACK]",
      "spl_version": "104",
      "published_date": "2026-06-01"
    }
  },
  "productid": "68071-4260_1a3c49be-c43a-da6c-e063-6394a90a39bf",
  "productndc": "68071-4260",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076639",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 250MG BASE",
        "product_no": "001",
        "approval_date": "Sep 10, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "002",
        "approval_date": "Sep 10, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 750MG BASE",
        "product_no": "003",
        "approval_date": "Sep 10, 2004"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CIPROFLOXACIN HYDROCHLORIDE",
  "proprietary_name": "ciprofloxacin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076639",
  "marketing_category": "ANDA",
  "nonproprietary_name": "ciprofloxacin",
  "start_marketing_date": "20040910",
  "active_numerator_strength": "250"
}

Related drugs

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