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
7133511520
7 TABLET, COATED in 1 BOTTLE (71335-1152-0)
ndc11
7133511521
20 TABLET, COATED in 1 BOTTLE (71335-1152-1)
ndc11
7133511522
10 TABLET, COATED in 1 BOTTLE (71335-1152-2)
ndc11
7133511523
14 TABLET, COATED in 1 BOTTLE (71335-1152-3)
ndc11
7133511524
6 TABLET, COATED in 1 BOTTLE (71335-1152-4)
ndc11
7133511525
30 TABLET, COATED in 1 BOTTLE (71335-1152-5)
ndc11
7133511526
60 TABLET, COATED in 1 BOTTLE (71335-1152-6)
ndc11
7133511527
12 TABLET, COATED in 1 BOTTLE (71335-1152-7)
ndc11
7133511528
40 TABLET, COATED in 1 BOTTLE (71335-1152-8)
ndc11
7133511529
90 TABLET, COATED in 1 BOTTLE (71335-1152-9)

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": "71335-1152_3bc30d61-cfc5-4855-834d-d82b9f9e040a",
  "productndc": "71335-1152",
  "dosage_form": "TABLET, COATED",
  "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": "Ciprofloxacin Tablets",
  "start_marketing_date": "20190713",
  "active_numerator_strength": "250"
}

Related drugs

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