ciprofloxacin

Orange BookUNIISPLATC J01MA02

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

Identification

ManufacturerProficient Rx LP

CountryUS (United States)

ATC codeJ01MA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
6318714206
6 TABLET in 1 BOTTLE (63187-142-06)
ndc11
6318714210
10 TABLET in 1 BOTTLE (63187-142-10)
ndc11
6318714214
14 TABLET in 1 BOTTLE (63187-142-14)
ndc11
6318714220
20 TABLET in 1 BOTTLE (63187-142-20)
ndc11
6318714228
28 TABLET in 1 BOTTLE (63187-142-28)
ndc11
6318714230
30 TABLET in 1 BOTTLE (63187-142-30)
ndc11
6318714260
60 TABLET in 1 BOTTLE (63187-142-60)
ndc11
6318714290
90 TABLET in 1 BOTTLE (63187-142-90)

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": "63187-142_91f426fc-3fc4-4c2f-a56d-10862e54d745",
  "productndc": "63187-142",
  "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"
}

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