Ciprofloxacin

Orange BookUNIISPLATC J01MA02

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

Identification

ManufacturerNorthwind Health Company, LLC

CountryUS (United States)

ATC codeJ01MA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
5165521620
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20)
ndc11
5165521625
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25)
ndc11
5165521652
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52)
ndc11
5165521653
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53)
ndc11
5165521684
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84)
ndc11
5165521687
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87)

Annotations

UNII (FDA Substance ID)

4BA73M5E37

CIPROFLOXACIN HYDROCHLORIDE

RxCUI 81981

Orange Book

A077859

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": "51655-216_48d2ac12-e669-d797-e063-6394a90aaa7f",
  "productndc": "51655-216",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077859",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 250MG BASE",
        "product_no": "001",
        "approval_date": "Apr 26, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "002",
        "approval_date": "Apr 26, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 750MG BASE",
        "product_no": "003",
        "approval_date": "Apr 26, 2007"
      }
    ],
    "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": "ANDA077859",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ciprofloxacin Hydrochloride",
  "start_marketing_date": "20230317",
  "active_numerator_strength": "500"
}

Related drugs

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