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United States · US · US:71335-2276_bee64582-e61e-4d78-9dc1-a1107ccc5f03
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
- ndc11713352276090 TABLET, FILM COATED in 1 BOTTLE (71335-2276-0)
- ndc11713352276130 TABLET, FILM COATED in 1 BOTTLE (71335-2276-1)
- ndc11713352276210 TABLET, FILM COATED in 1 BOTTLE (71335-2276-2)
- ndc1171335227637 TABLET, FILM COATED in 1 BOTTLE (71335-2276-3)
- ndc11713352276414 TABLET, FILM COATED in 1 BOTTLE (71335-2276-4)
- ndc1171335227655 TABLET, FILM COATED in 1 BOTTLE (71335-2276-5)
- ndc11713352276620 TABLET, FILM COATED in 1 BOTTLE (71335-2276-6)
- ndc11713352276760 TABLET, FILM COATED in 1 BOTTLE (71335-2276-7)
- ndc1171335227683 TABLET, FILM COATED in 1 BOTTLE (71335-2276-8)
- ndc11713352276950 TABLET, FILM COATED in 1 BOTTLE (71335-2276-9)
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": "71335-2276_bee64582-e61e-4d78-9dc1-a1107ccc5f03",
"productndc": "71335-2276",
"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": "500"
}Related drugs
Other records sharing ATC code J01MA12.
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