Ciprofloxacin

Orange BookUNIISPLATC J01MA02

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeJ01MA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 10

ndc11
7133518670
7 TABLET, FILM COATED in 1 BOTTLE (71335-1867-0)
ndc11
7133518671
20 TABLET, FILM COATED in 1 BOTTLE (71335-1867-1)
ndc11
7133518672
10 TABLET, FILM COATED in 1 BOTTLE (71335-1867-2)
ndc11
7133518673
14 TABLET, FILM COATED in 1 BOTTLE (71335-1867-3)
ndc11
7133518674
6 TABLET, FILM COATED in 1 BOTTLE (71335-1867-4)
ndc11
7133518675
30 TABLET, FILM COATED in 1 BOTTLE (71335-1867-5)
ndc11
7133518676
60 TABLET, FILM COATED in 1 BOTTLE (71335-1867-6)
ndc11
7133518677
12 TABLET, FILM COATED in 1 BOTTLE (71335-1867-7)
ndc11
7133518678
40 TABLET, FILM COATED in 1 BOTTLE (71335-1867-8)
ndc11
7133518679
90 TABLET, FILM COATED in 1 BOTTLE (71335-1867-9)

Annotations

UNII (FDA Substance ID)

4BA73M5E37

CIPROFLOXACIN HYDROCHLORIDE

RxCUI 81981

Orange Book

A076558

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": "71335-1867_6ef39f10-95be-4fc5-b917-d8e9f5e8e05c",
  "productndc": "71335-1867",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "076558",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 250MG BASE",
        "product_no": "002",
        "approval_date": "Jun 9, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "003",
        "approval_date": "Jun 9, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 750MG BASE",
        "product_no": "004",
        "approval_date": "Jun 9, 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": "ANDA076558",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ciprofloxacin",
  "start_marketing_date": "20040609",
  "active_numerator_strength": "250"
}

Related drugs

Other records sharing ATC code J01MA02.

Access this data programmatically

Query Ciprofloxacin and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs