levofloxacin

Product NDC
71335-2276
11-digit product format
713352276
Labeler code
71335
Product ID
71335-2276_bee64582-e61e-4d78-9dc1-a1107ccc5f03
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
levofloxacin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077652
Marketing category
ANDA
Marketing start
2022-01-10
Substance
LEVOFLOXACIN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
6GNT3Y5LMFLEVOFLOXACIN138199-71-0LEVOFLOXACIN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2276-07133522760090 TABLET, FILM COATED in 1 BOTTLE (71335-2276-0) 2024-07-16NoNoHistorical
71335-2276-17133522760130 TABLET, FILM COATED in 1 BOTTLE (71335-2276-1) 2023-12-05NoNoHistorical
71335-2276-27133522760210 TABLET, FILM COATED in 1 BOTTLE (71335-2276-2) 2023-12-26NoNoHistorical
71335-2276-3713352276037 TABLET, FILM COATED in 1 BOTTLE (71335-2276-3) 2024-07-16NoNoHistorical
71335-2276-47133522760414 TABLET, FILM COATED in 1 BOTTLE (71335-2276-4) 2023-11-27NoNoHistorical
71335-2276-5713352276055 TABLET, FILM COATED in 1 BOTTLE (71335-2276-5) 2024-07-16NoNoHistorical
71335-2276-67133522760620 TABLET, FILM COATED in 1 BOTTLE (71335-2276-6) 2024-07-16NoNoHistorical
71335-2276-77133522760760 TABLET, FILM COATED in 1 BOTTLE (71335-2276-7) 2024-07-16NoNoHistorical
71335-2276-8713352276083 TABLET, FILM COATED in 1 BOTTLE (71335-2276-8) 2023-12-05NoNoHistorical
71335-2276-97133522760950 TABLET, FILM COATED in 1 BOTTLE (71335-2276-9) 2024-07-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
levofloxacinBryant Ranch Prepack2024-08-26HUMAN PRESCRIPTION DRUG LABEL102