ENALAPRIL MALEATE

Product NDC: 51655-279
11-digit product format: 516550279
Labeler code: 51655
Product ID: 51655-279_978f67f2-e58a-4843-b1a5-892b60a0a1f5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ENALAPRIL MALEATE
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA075483
Marketing category: ANDA
Marketing start: 2014-12-09
Marketing end: 0000-00-00
Substance: ENALAPRIL MALEATE
Active strength: 20 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: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-279-52	2026-01-08	C162847	48780-1	9d75b9d0-e9cb-f424-e053-dadaa90a57ce	68b3ad34-adbe-4c9a-b8f3-be80f8e413ed
51655-279-52	2020-01-31	C162847	48780-1	9d75b9d0-e9cb-f424-e053-dadaa90a57ce	68b3ad34-adbe-4c9a-b8f3-be80f8e413ed

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ENALAPRIL MALEATE	ACTIVE INGREDIENT	9O25354EPJ	ENALAPRIL MALEATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
ENALAPRILAT ANHYDROUS	ACTIVE MOIETY	Q508Q118JM	ENALAPRIL MALEATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-279	ENALAPRIL MALEATE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20141210_68b3ad34-adbe-4c9a-b8f3-be80f8e413ed.zip