Furosemide

Product NDC
35356-873
11-digit product format
353560873
Labeler code
35356
Product ID
35356-873_362485bb-0de7-4bc7-90e2-4bcc5e7b425a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-873-30EA - Each35356-8739f1e4c85-c69e-45fe-95c2-0529a5f6327212013-08-02
35356-873-90EA - Each35356-8730062a80a-3a10-43b7-8e02-46e1f0db1fcf12013-09-04