Lisinopril with Hydrochlorothiazide

Product NDC
66267-751
11-digit product format
662670751
Labeler code
66267
Product ID
66267-751_9cbeac96-537c-3898-e053-2995a90aae67
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
66267-751-30EA - Each66267-751c8d0b31a-ef70-4634-9b58-8e2321e6453112017-03-06
66267-751-90EA - Each66267-7515eadb28b-ef56-4c33-a231-2aa2e890d3e112017-03-06