Nitrofurantoin Monohydrate/ Macrocrystalline

Product NDC
50090-0866
11-digit product format
500900866
Labeler code
50090
Product ID
50090-0866_37bed24f-a80d-4633-a776-cc8f56c4cb0f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nitrofurantoin Monohydrate/Macrocrystalline
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA020064
Marketing category
NDA
Marketing start
2011-05-25
Marketing end
0000-00-00
Substance
NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE
Active strength
25 mg/1; mg/1
Pharmacologic classes
Nitrofurans [CS],Nitrofuran Antibacterial [EPC],Nitrofurans [CS],Nitrofuran Antibacterial [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0866-0EA - Each50090-0866abee11e8-a0af-4807-bba9-4385c473fd1912018-10-11
50090-0866-1EA - Each50090-08664568a146-af9c-4595-a579-7bc08fbe301512021-08-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-0866NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALLINE (NITROFURANTOIN MONOHYDRATE/MACROCRYSTALLINE) CAPSULE [A-S MEDICATION SOLUTIONS]16Legacy NDC20230623_04c34f1d-6b20-48ed-b884-ef8fa34d25ff.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-0866-05009008660014 CAPSULE in 1 BOTTLE (50090-0866-0) 14 capsule2014-11-280000-00-00NoNoCurrent
50090-0866-15009008660110 CAPSULE in 1 BOTTLE (50090-0866-1) 10 capsule2020-08-140000-00-00NoNoCurrent