Fluconazole

Product NDC
71335-1511
11-digit product format
713351511
Labeler code
71335
Product ID
71335-1511_50772307-3892-46b3-95b1-02bcd54c4695
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluconazole
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076077
Marketing category
ANDA
Marketing start
2004-07-29
Marketing end
2022-06-30
Substance
FLUCONAZOLE
Active strength
200 mg/1
Pharmacologic classes
Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1511-0713351511004 TABLET in 1 BOTTLE (71335-1511-0) 4 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-17133515110130 TABLET in 1 BOTTLE (71335-1511-1) 30 tablet2020-02-142022-06-30NoNoCurrent
71335-1511-27133515110212 TABLET in 1 BOTTLE (71335-1511-2) 12 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-371335151103100 TABLET in 1 BOTTLE (71335-1511-3) 100 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-4713351511043 TABLET in 1 BOTTLE (71335-1511-4) 3 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-57133515110528 TABLET in 1 BOTTLE (71335-1511-5) 28 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-6713351511061 TABLET in 1 BOTTLE (71335-1511-6) 1 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-7713351511072 TABLET in 1 BOTTLE (71335-1511-7) 2 tablet2020-06-012022-06-30NoNoCurrent
71335-1511-87133515110814 TABLET in 1 BOTTLE (71335-1511-8) 14 tablet2021-12-282022-06-30NoNoCurrent
71335-1511-9713351511098 TABLET in 1 BOTTLE (71335-1511-9) 8 tablet2021-12-282022-06-30NoNoCurrent