Fuosemide

Product NDC
0615-7938
11-digit product format
006157938
Labeler code
0615
Product ID
0615-7938_8676925e-cabd-4690-9632-afed4b1211c9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
NDA018823
Marketing category
NDA
Marketing start
1983-11-10
Marketing end
2022-10-31
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
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0615-7938-050061579380515 TABLET in 1 BLISTER PACK (0615-7938-05) 15 tablet2016-04-042022-09-30NoNoCurrent
0615-7938-07006157938077 TABLET in 1 BLISTER PACK (0615-7938-07) 7 tablet2018-07-032022-09-30NoNoCurrent
0615-7938-140061579381414 TABLET in 1 BLISTER PACK (0615-7938-14) 14 tablet2018-07-032022-09-30NoNoCurrent
0615-7938-280061579382828 TABLET in 1 BLISTER PACK (0615-7938-28) 28 tablet2018-07-032022-09-30NoNoCurrent
0615-7938-30006157938306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7938-30) > 5 TABLET in 1 BLISTER PACK6 blister pack2016-04-112022-10-31NoNoCurrent
0615-7938-390061579383930 TABLET in 1 BLISTER PACK (0615-7938-39) 30 tablet2016-04-042022-09-30NoNoCurrent