Triamterene and Hydrochlorothiazide

Product NDC
68788-6996
11-digit product format
687886996
Labeler code
68788
Product ID
68788-6996_91e14171-a237-4d0d-8024-c2d3ccf8c842
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triamterene and Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA071251
Marketing category
ANDA
Marketing start
2020-06-01
Marketing end
0000-00-00
Substance
TRIAMTERENE; HYDROCHLOROTHIAZIDE
Active strength
75 mg/1; mg/1
Pharmacologic classes
Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-6996-168788699601100 TABLET in 1 BOTTLE (68788-6996-1) 100 tablet2020-06-010000-00-00NoNoCurrent
68788-6996-36878869960330 TABLET in 1 BOTTLE (68788-6996-3) 30 tablet2020-06-010000-00-00NoNoCurrent
68788-6996-66878869960660 TABLET in 1 BOTTLE (68788-6996-6) 60 tablet2020-06-010000-00-00NoNoCurrent
68788-6996-96878869960990 TABLET in 1 BOTTLE (68788-6996-9) 90 tablet2020-06-010000-00-00NoNoCurrent