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
7133500700
7 TABLET in 1 BOTTLE (71335-0070-0)
ndc11
7133500701
14 TABLET in 1 BOTTLE (71335-0070-1)
ndc11
7133500702
30 TABLET in 1 BOTTLE (71335-0070-2)
ndc11
7133500703
20 TABLET in 1 BOTTLE (71335-0070-3)
ndc11
7133500704
60 TABLET in 1 BOTTLE (71335-0070-4)
ndc11
7133500705
6 TABLET in 1 BOTTLE (71335-0070-5)
ndc11
7133500706
10 TABLET in 1 BOTTLE (71335-0070-6)
ndc11
7133500707
28 TABLET in 1 BOTTLE (71335-0070-7)
ndc11
7133500708
100 TABLET in 1 BOTTLE (71335-0070-8)
ndc11
7133500709
40 TABLET in 1 BOTTLE (71335-0070-9)

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": "71335-0070_7e450b73-3a77-48fb-8552-4d85d44f966f",
  "productndc": "71335-0070",
  "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": "500"
}

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