Furosemide

Product NDC
50090-3339
11-digit product format
500903339
Labeler code
50090
Product ID
50090-3339_be05fc5d-5269-4c38-b749-483b6f6b8f32
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA076796
Marketing category
ANDA
Marketing start
2004-03-26
Marketing end
0000-00-00
Substance
FUROSEMIDE
Active strength
40 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
50090-3339-0EA - Each50090-33390bbaaade-c6b6-4e53-8e42-48ef727d2e8c12019-05-02
50090-3339-1EA - Each50090-3339f6582527-2535-4d37-b0a2-d0ddfde120b112019-05-02
50090-3339-3EA - Each50090-3339632e3063-251c-42cb-8738-79a1fd77cab312021-09-07
50090-3339-9EA - Each50090-3339f3a76c38-d9f8-4950-a0d4-2ea529cd231a12019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3339-05009033390030 TABLET in 1 BOTTLE, PLASTIC (50090-3339-0) 30 tablet2018-01-190000-00-00NoNoCurrent
50090-3339-150090333901100 TABLET in 1 BOTTLE (50090-3339-1) 100 tablet2018-01-290000-00-00NoNoCurrent
50090-3339-35009033390360 TABLET in 1 BOTTLE, PLASTIC (50090-3339-3) 60 tablet2014-11-280000-00-00NoNoCurrent
50090-3339-95009033390990 TABLET in 1 BOTTLE (50090-3339-9) 90 tablet2018-01-190000-00-00NoNoCurrent