Nitrofurantoin

Product NDC
71335-1374
11-digit product format
713351374
Labeler code
71335
Product ID
71335-1374_25e88236-f6d3-45ea-8766-8e50f4862d66
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nitrofurantoin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091095
Marketing category
ANDA
Marketing start
2015-10-01
Marketing end
0000-00-00
Substance
NITROFURANTOIN
Active strength
50 mg/1
Pharmacologic classes
Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1374-17133513740128 CAPSULE in 1 BOTTLE (71335-1374-1) 28 capsule2019-10-220000-00-00NoNoCurrent
71335-1374-27133513740240 CAPSULE in 1 BOTTLE (71335-1374-2) 40 capsule2019-10-220000-00-00NoNoCurrent
71335-1374-37133513740320 CAPSULE in 1 BOTTLE (71335-1374-3) 20 capsule2019-10-220000-00-00NoNoCurrent
71335-1374-47133513740490 CAPSULE in 1 BOTTLE (71335-1374-4) 90 capsule2019-10-220000-00-00NoNoCurrent
71335-1374-57133513740530 CAPSULE in 1 BOTTLE (71335-1374-5) 30 capsule2019-10-220000-00-00NoNoCurrent
71335-1374-67133513740612 CAPSULE in 1 BOTTLE (71335-1374-6) 12 capsule2019-10-220000-00-00NoNoCurrent