LATANOPROST

Orange BookUNIISPLATC S01EE01

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

Identification

ManufacturerRising Pharma Holdings, Inc.

CountryUS (United States)

ATC codeS01EE01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6498051625
1 BOTTLE, DROPPER in 1 CARTON (64980-516-25) / 2.5 mL in 1 BOTTLE, DROPPER

Annotations

UNII (FDA Substance ID)

6Z5B6HVF6O

LATANOPROST

RxCUI 43611

Orange Book

A202442

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6Z5B6HVF6O",
    "rxcui": "43611",
    "inchikey": "GGXICVAJURFBLW-CEYXHVGTSA-N",
    "display_name": "LATANOPROST",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "be74d517-7f73-a74c-e053-2a95a90a3819": {
      "match": "brand_token",
      "title": "LATANOPROST SOLUTION/ DROPS [NUCARE PHARMACEUTICALS,INC.]",
      "spl_version": "2",
      "published_date": "2026-03-09"
    }
  },
  "productid": "64980-516_c9d37a89-f385-4cd5-9a18-15abc5ba2dd9",
  "productndc": "64980-516",
  "dosage_form": "SOLUTION",
  "orange_book": {
    "appl_no": "202442",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AT",
        "strength": "0.005%",
        "product_no": "001",
        "approval_date": "Apr 22, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LATANOPROST",
  "proprietary_name": "LATANOPROST",
  "active_ingred_unit": "ug/mL",
  "application_number": "ANDA202442",
  "marketing_category": "ANDA",
  "nonproprietary_name": "latanoprost",
  "start_marketing_date": "20160901",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code S01EE01.

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