Hydrochlorothiazide

Product NDC
55700-301
11-digit product format
557000301
Labeler code
55700
Product ID
55700-301_239eca3e-bee6-460f-a55f-0f06afec2d38
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA202556
Marketing category
ANDA
Marketing start
2013-04-10
Marketing end
0000-00-00
Substance
HYDROCHLOROTHIAZIDE
Active strength
25 mg/1
Pharmacologic classes
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
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
55700-301-30EA - Each55700-30171dd64e3-b276-4e11-9615-0d5e8e75da4012016-05-16
55700-301-60EA - Each55700-30177b8c3e5-78c3-4cd5-b942-361955f1206612017-05-04
55700-301-90EA - Each55700-301c8686c0d-ae31-42b4-8087-82689bf4db4c12016-05-16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-301-605570003016060 TABLET in 1 BOTTLE (55700-301-60) 60 tablet2017-03-100000-00-00NoNoCurrent
55700-301-905570003019090 TABLET in 1 BOTTLE (55700-301-90) 90 tablet2016-01-130000-00-00NoNoCurrent