Triamterene hydrochlorothiazide

Product NDC
43063-442
11-digit product format
430630442
Labeler code
43063
Product ID
43063-442_a900c99c-99f1-f63b-e053-2a95a90a872d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triamterene and hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA072011
Marketing category
ANDA
Marketing start
1988-06-17
Marketing end
2020-11-30
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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-442-90EA - Each43063-44278b38870-cbbd-410f-bb9f-2f0d61081b5d12013-05-02