Nitrofurantion

Product NDC
71335-0793
11-digit product format
713350793
Labeler code
71335
Product ID
71335-0793_da6ffee4-51bd-410c-958c-c45f9b68b029
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nitrofurantion
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA201722
Marketing category
ANDA
Marketing start
2016-04-15
Marketing end
0000-00-00
Substance
NITROFURANTOIN
Active strength
50 mg/1
Pharmacologic classes
Nitrofuran Antibacterial [EPC], Nitrofurans [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0793-17133507930128 CAPSULE in 1 BOTTLE (71335-0793-1) 28 capsule2018-04-300000-00-00NoNoCurrent
71335-0793-27133507930240 CAPSULE in 1 BOTTLE (71335-0793-2) 40 capsule2018-04-300000-00-00NoNoCurrent
71335-0793-37133507930320 CAPSULE in 1 BOTTLE (71335-0793-3) 20 capsule2018-04-300000-00-00NoNoCurrent
71335-0793-47133507930490 CAPSULE in 1 BOTTLE (71335-0793-4) 90 capsule2018-04-300000-00-00NoNoCurrent
71335-0793-57133507930530 CAPSULE in 1 BOTTLE (71335-0793-5) 30 capsule2018-04-300000-00-00NoNoCurrent
71335-0793-67133507930612 CAPSULE in 1 BOTTLE (71335-0793-6) 12 capsule2018-04-300000-00-00NoNoCurrent