Lisinopril with Hydrochlorothiazide

Product NDC
50090-2086
11-digit product format
500902086
Labeler code
50090
Product ID
50090-2086_a3c74d1e-c985-4bc5-b3e0-838d1f803136
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril and Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2086-0EA - Each50090-2086d8c0b8d7-fb11-4d30-bf4d-5a9e83cd44f012019-02-13
50090-2086-1EA - Each50090-208638263845-c6ad-4f84-b128-d83115a88aac12019-02-13