Fosinopril Sodium and Hydrochlorothiazide

Product NDC
68462-554
11-digit product format
684620554
Labeler code
68462
Product ID
68462-554_794e6638-9b32-49d3-988b-3c0f681bac12
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fosinopril Sodium and Hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Glenmark Pharmaceuticals Inc., USA
Application
ANDA090228
Marketing category
ANDA
Marketing start
2009-07-09
Marketing end
0000-00-00
Substance
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Active strength
10 mg/1; mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
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
68462-554-01EA - Each68462-5548a92eebf-ffe9-4106-b402-0e1f704b0ecb12012-07-24

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68462-554-0168462055401100 TABLET in 1 BOTTLE (68462-554-01) 100 tablet2009-07-090000-00-00NoNoCurrent
68462-554-10684620554101000 TABLET in 1 BOTTLE (68462-554-10) 1000 tablet2009-07-090000-00-00NoNoCurrent
68462-554-306846205543030 TABLET in 1 BOTTLE (68462-554-30) 30 tablet2009-07-090000-00-00NoNoCurrent