Lisinopril with Hydrochlorothiazide

Product NDC
66267-752
11-digit product format
662670752
Labeler code
66267
Product ID
66267-752_9cbd76c6-78f5-4e58-e053-2a95a90a2347
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril and Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA076265
Marketing category
ANDA
Marketing start
2002-07-08
Marketing end
0000-00-00
Substance
HYDROCHLOROTHIAZIDE; LISINOPRIL
Active strength
13 mg/1; mg/1
Pharmacologic classes
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-752-30EA - Each66267-752f507d849-fd26-44a7-8614-0ece3eb0908412017-03-06
66267-752-90EA - Each66267-7520ebcdf84-2721-4526-a589-b5f549a2d65312017-03-06