Enalapril Maleate

Product NDC
68788-7275
11-digit product format
687887275
Labeler code
68788
Product ID
68788-7275_41d0d6f4-4cd8-4a0c-9512-7a90a030a28f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Enalapril Maleate
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
NDA018998
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2019-01-08
Marketing end
0000-00-00
Substance
ENALAPRIL MALEATE
Active strength
5 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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7275-1EA - Each68788-7275babc2f92-3a31-4911-956b-fdb4a2f666c512019-04-11
68788-7275-3EA - Each68788-7275fd10252c-37cf-4890-a473-440cf34c427112019-04-11
68788-7275-6EA - Each68788-7275e27a7252-dbce-402a-b5d7-1c7fb885ce6612019-04-11
68788-7275-9EA - Each68788-727583b2dd23-a350-4ed1-b306-ff2a2d729c3a12019-04-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7275-168788727501100 TABLET in 1 BOTTLE (68788-7275-1) 100 tablet2019-01-080000-00-00NoNoCurrent
68788-7275-36878872750330 TABLET in 1 BOTTLE (68788-7275-3) 30 tablet2019-01-080000-00-00NoNoCurrent
68788-7275-66878872750660 TABLET in 1 BOTTLE (68788-7275-6) 60 tablet2019-01-080000-00-00NoNoCurrent
68788-7275-96878872750990 TABLET in 1 BOTTLE (68788-7275-9) 90 tablet2019-01-080000-00-00NoNoCurrent