Hydrochlorothiazide

Product NDC
55700-758
11-digit product format
557000758
Labeler code
55700
Product ID
55700-758_f6541cb4-3dc1-4361-a082-c7be318cbf35
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA083177
Marketing category
ANDA
Marketing start
2019-05-24
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
55700-758-30EA - Each55700-7580b5de518-f573-4f02-a96e-b9313843826512019-06-19
55700-758-90EA - Each55700-75839184f8b-464e-4588-9e23-af4977f5722c12019-06-19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-758-305570007583030 TABLET in 1 BOTTLE (55700-758-30) 30 tablet2019-05-240000-00-00NoNoCurrent
55700-758-905570007589090 TABLET in 1 BOTTLE (55700-758-90) 90 tablet2019-05-240000-00-00NoNoCurrent