Hydrochlorothiazide

Product NDC
67544-346
11-digit product format
675440346
Labeler code
67544
Product ID
67544-346_5d3ad7cd-d844-49b9-adde-a05f12d0ea8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA040412
Marketing category
ANDA
Marketing start
2002-03-29
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
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
67544-346-15EA - Each67544-346dae23188-9c8b-459b-ac57-c0aaaa1c745812014-07-02
67544-346-30EA - Each67544-3461dce573c-ed17-4588-a5a7-33c7fd4abee012014-07-02
67544-346-45EA - Each67544-34654768b37-c2b6-4380-8219-ef780244952912014-07-02
67544-346-60EA - Each67544-346c090a5e8-11d0-410c-b2e4-1ea460e7b85c12014-07-02
67544-346-65EA - Each67544-346b592769b-7ca3-469d-be67-c369b5b2fe4112014-09-03