Enalapril Maleate

Product NDC
71335-1854
11-digit product format
713351854
Labeler code
71335
Product ID
71335-1854_75272d12-c820-4436-9551-c65b692efa3d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Enalapril Maleate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075657
Marketing category
ANDA
Marketing start
2001-01-23
Marketing end
0000-00-00
Substance
ENALAPRIL MALEATE
Active strength
10 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1854ENALAPRIL MALEATE TABLET [BRYANT RANCH PREPACK]101Legacy NDC20240518_ee57b3f6-0f0d-45ae-b7ca-1b06fefb045f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1854-17133518540160 TABLET in 1 BOTTLE (71335-1854-1) 60 tablet2021-12-210000-00-00NoNoCurrent
71335-1854-27133518540230 TABLET in 1 BOTTLE (71335-1854-2) 30 tablet2021-12-210000-00-00NoNoCurrent
71335-1854-371335185403100 TABLET in 1 BOTTLE (71335-1854-3) 100 tablet2021-12-210000-00-00NoNoCurrent
71335-1854-47133518540490 TABLET in 1 BOTTLE (71335-1854-4) 90 tablet2021-12-210000-00-00NoNoCurrent
71335-1854-571335185405120 TABLET in 1 BOTTLE (71335-1854-5) 120 tablet2021-12-210000-00-00NoNoCurrent