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United States · US · US:71335-2265_477d7d9e-1637-4c49-b588-f1da546a67f0
levofloxacin
Orange BookUNIISPLATC J01MA12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeJ01MA12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc1171335226503 TABLET, FILM COATED in 1 BOTTLE (71335-2265-0)
- ndc11713352265110 TABLET, FILM COATED in 1 BOTTLE (71335-2265-1)
- ndc11713352265230 TABLET, FILM COATED in 1 BOTTLE (71335-2265-2)
- ndc1171335226537 TABLET, FILM COATED in 1 BOTTLE (71335-2265-3)
- ndc11713352265420 TABLET, FILM COATED in 1 BOTTLE (71335-2265-4)
- ndc1171335226555 TABLET, FILM COATED in 1 BOTTLE (71335-2265-5)
- ndc11713352265614 TABLET, FILM COATED in 1 BOTTLE (71335-2265-6)
- ndc11713352265728 TABLET, FILM COATED in 1 BOTTLE (71335-2265-7)
- ndc11713352265860 TABLET, FILM COATED in 1 BOTTLE (71335-2265-8)
- ndc11713352265990 TABLET, FILM COATED in 1 BOTTLE (71335-2265-9)
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": "71335-2265_477d7d9e-1637-4c49-b588-f1da546a67f0",
"productndc": "71335-2265",
"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": "20220110",
"active_numerator_strength": "750"
}Related drugs
Other records sharing ATC code J01MA12.
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