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United States · US · US:71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52

Ciprofloxacin

Orange BookUNIISPLATC J01MA02

Last synced from FDA National Drug Code directory (United States) on

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
    7133524500
    7 TABLET in 1 BOTTLE (71335-2450-0)
  • ndc11
    7133524501
    14 TABLET in 1 BOTTLE (71335-2450-1)
  • ndc11
    7133524502
    30 TABLET in 1 BOTTLE (71335-2450-2)
  • ndc11
    7133524503
    20 TABLET in 1 BOTTLE (71335-2450-3)
  • ndc11
    7133524504
    60 TABLET in 1 BOTTLE (71335-2450-4)
  • ndc11
    7133524505
    6 TABLET in 1 BOTTLE (71335-2450-5)
  • ndc11
    7133524506
    10 TABLET in 1 BOTTLE (71335-2450-6)
  • ndc11
    7133524507
    28 TABLET in 1 BOTTLE (71335-2450-7)
  • ndc11
    7133524508
    100 TABLET in 1 BOTTLE (71335-2450-8)
  • ndc11
    7133524509
    40 TABLET in 1 BOTTLE (71335-2450-9)

Annotations

UNII (FDA Substance ID)
4BA73M5E37
CIPROFLOXACIN HYDROCHLORIDE
RxCUI 81981
Orange Book
A208921
ABAB
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": "71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52",
  "productndc": "71335-2450",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "208921",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 250MG BASE",
        "product_no": "001",
        "approval_date": "Jun 22, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "002",
        "approval_date": "Jun 22, 2018"
      }
    ],
    "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": "ANDA208921",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ciprofolxacin",
  "start_marketing_date": "20231001",
  "active_numerator_strength": "500"
}

Related drugs

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