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United States · US · US:50090-0882_4f560092-60a1-41f4-85a8-279dc97c81da

Ciprofloxacin Hydrochloride

Orange BookUNIISPLATC J01MA02

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

Identification

ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeJ01MA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5009008820
    1 BOTTLE, PLASTIC in 1 CARTON (50090-0882-0) / 5 mL in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
4BA73M5E37
CIPROFLOXACIN HYDROCHLORIDE
RxCUI 81981
Orange Book
N019992
AT
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": "OPHTHALMIC",
  "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": "50090-0882_4f560092-60a1-41f4-85a8-279dc97c81da",
  "productndc": "50090-0882",
  "dosage_form": "SOLUTION/ DROPS",
  "orange_book": {
    "appl_no": "019992",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AT",
        "strength": "EQ 0.3% BASE",
        "product_no": "001",
        "approval_date": "Dec 31, 1990"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CIPROFLOXACIN HYDROCHLORIDE",
  "proprietary_name": "Ciprofloxacin Hydrochloride",
  "active_ingred_unit": "mg/mL",
  "application_number": "NDA019992",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "Ciprofloxacin Hydrochloride",
  "start_marketing_date": "20040507",
  "active_numerator_strength": "3"
}

Related drugs

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