Furosemide

Product NDC
49999-030
11-digit product format
499990030
Labeler code
49999
Product ID
49999-030_a0c7cfb2-b022-4376-a330-bec0ab3d9248
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
NDA018569
Marketing category
NDA
Marketing start
2011-11-28
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
49999-030-00EA - Each49999-0309e08d857-e132-43ac-8171-9f92c34f563612012-07-24
49999-030-10EA - Each49999-030d41f9a1f-cb74-4b67-bba8-6b680ed4fcdc12012-07-24
49999-030-30EA - Each49999-030b26049c1-d1bc-49e9-9d10-7d33a864f9f912012-07-24
49999-030-60EA - Each49999-030ee3460ed-3c19-4fc1-a36d-512b171511a512012-07-24
49999-030-90EA - Each49999-0307c0d2c6f-358c-4924-b680-84a4e7b647ec12012-07-24