Furosemide

Product NDC
55700-461
11-digit product format
557000461
Labeler code
55700
Product ID
55700-461_a09d16f5-d349-436e-a872-3642d6e92631
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Quality Care Products LLC
Application
ANDA077293
Marketing category
ANDA
Marketing start
2006-02-01
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
2023-12-31
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
55700-461-30EA - Each55700-46157202204-4226-4b2b-ba0a-d922ff2431cd12017-03-06
55700-461-60EA - Each55700-4617ffbcdc0-b3bc-450f-867a-2186307d571f12017-03-06
55700-461-90EA - Each55700-461d843ef61-cafa-431f-b935-e22e2ea33c9c12018-06-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-461-305570004613030 TABLET in 1 BOTTLE (55700-461-30) 30 tablet2016-09-020000-00-00NoNoCurrent