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United States · US · US:72789-108_4d622f0c-9f42-a920-e063-6394a90a0f73

Ciprofloxacin

Orange BookUNIISPLATC J01MA02

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

Identification

ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeJ01MA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7278910802
    2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-02)
  • ndc11
    7278910810
    10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-10)
  • ndc11
    7278910814
    14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-14)
  • ndc11
    7278910820
    20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-20)
  • ndc11
    7278910828
    28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-28)
  • ndc11
    7278910830
    30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-30)

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": "72789-108_4d622f0c-9f42-a920-e063-6394a90a0f73",
  "productndc": "72789-108",
  "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": "500"
}

Related drugs

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