Furosemide

Product NDC
50090-3338
11-digit product format
500903338
Labeler code
50090
Product ID
50090-3338_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
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
50090-3338-0EA - Each50090-3338c88ac35e-15fb-4ed1-9e8e-a685b6ce862712019-05-02
50090-3338-1EA - Each50090-3338f81e79d2-fcdd-4e4e-bfa8-8490aeeee08012019-05-02
50090-3338-7EA - Each50090-333800bc70ef-cc57-4084-961a-60acc4f6f0d712019-05-02
50090-3338-8EA - Each50090-333804cb5b0f-80aa-4224-b0da-de85b993baff12019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3338-05009033380030 TABLET in 1 BOTTLE, PLASTIC (50090-3338-0) 30 tablet2018-04-250000-00-00NoNoCurrent
50090-3338-150090333801100 TABLET in 1 BOTTLE (50090-3338-1) 100 tablet2018-01-190000-00-00NoNoCurrent
50090-3338-750090333807200 TABLET in 1 BOTTLE (50090-3338-7) 200 tablet2018-05-250000-00-00NoNoCurrent
50090-3338-85009033380890 TABLET in 1 BOTTLE (50090-3338-8) 90 tablet2018-01-190000-00-00NoNoCurrent