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United States · US · US:68788-8809_927873c8-8c69-424c-84f4-279ea976ae67

levofloxacin

Orange BookUNIISPLATC J01MA12

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

Identification

ManufacturerPreferred Pharmaceuticals Inc
CountryUS (United States)
ATC codeJ01MA12
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6878888091
    10 TABLET, FILM COATED in 1 BOTTLE (68788-8809-1)
  • ndc11
    6878888092
    20 TABLET, FILM COATED in 1 BOTTLE (68788-8809-2)
  • ndc11
    6878888094
    14 TABLET, FILM COATED in 1 BOTTLE (68788-8809-4)
  • ndc11
    6878888097
    7 TABLET, FILM COATED in 1 BOTTLE (68788-8809-7)

Annotations

UNII (FDA Substance ID)
6GNT3Y5LMF
LEVOFLOXACIN
RxCUI 82122
Orange Book
A077652
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6GNT3Y5LMF",
    "rxcui": "82122",
    "inchikey": "SUIQUYDRLGGZOL-RCWTXCDDSA-N",
    "display_name": "LEVOFLOXACIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "070375be-3b67-4299-ae8f-4a7b157ac16f": {
      "match": "brand_token",
      "title": "LEVOFLOXACIN TABLET, FILM COATED [CARDINAL HEALTH 107, LLC]",
      "spl_version": "19",
      "published_date": "2026-06-01"
    }
  },
  "productid": "68788-8809_927873c8-8c69-424c-84f4-279ea976ae67",
  "productndc": "68788-8809",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077652",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "250MG",
        "product_no": "001",
        "approval_date": "Sep 7, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "500MG",
        "product_no": "002",
        "approval_date": "Sep 7, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "750MG",
        "product_no": "003",
        "approval_date": "Sep 7, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LEVOFLOXACIN",
  "proprietary_name": "levofloxacin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077652",
  "marketing_category": "ANDA",
  "nonproprietary_name": "levofloxacin",
  "start_marketing_date": "20250120",
  "active_numerator_strength": "750"
}

Related drugs

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