Furosemide

Product NDC
50090-2560
11-digit product format
500902560
Labeler code
50090
Product ID
50090-2560_f77a8e1b-1413-4d21-9f3e-d03006d06de5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA018487
Marketing category
NDA
Marketing start
1981-08-27
Marketing end
0000-00-00
Substance
FUROSEMIDE
Active strength
20 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [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
50090-2560-0EA - Each50090-2560457d7921-2b8c-4f81-8962-aab7bb3fd74512019-04-11
50090-2560-1EA - Each50090-25600aff79eb-5b82-4b42-8813-ca89816970c112018-11-06
50090-2560-7EA - Each50090-256096002496-9d8f-49b4-8e04-2fe26533732712018-11-06
50090-2560-8EA - Each50090-2560247e26a8-4906-4c0f-aaa9-33d8b1ff157d12018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-2560-05009025600030 TABLET in 1 BOTTLE (50090-2560-0) 30 tablet2016-12-230000-00-00NoNoCurrent
50090-2560-150090256001100 TABLET in 1 BOTTLE (50090-2560-1) 100 tablet2016-11-010000-00-00NoNoCurrent
50090-2560-750090256007200 TABLET in 1 BOTTLE (50090-2560-7) 200 tablet2016-11-160000-00-00NoNoCurrent
50090-2560-85009025600890 TABLET in 1 BOTTLE (50090-2560-8) 90 tablet2016-10-260000-00-00NoNoCurrent