RAMIPRIL

Product NDC: 51655-117
11-digit product format: 516550117
Labeler code: 51655
Product ID: 51655-117_efbd9543-b8ae-43ef-8551-f0733760c751
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: RAMIPRIL
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA076549
Marketing category: ANDA
Marketing start: 2014-12-30
Marketing end: 0000-00-00
Substance: RAMIPRIL
Active strength: 5 mg/1
Pharmacologic classes: 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#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-117-52	2026-01-08	C162847	48780-1	9d75b9d0-0187-f424-e053-dadaa90a57ce	1a171aaf-e782-4c33-af9b-9806597b1d30
51655-117-52	2020-01-31	C162847	48780-1	9d75b9d0-0187-f424-e053-dadaa90a57ce	1a171aaf-e782-4c33-af9b-9806597b1d30

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
RAMIPRIL	ACTIVE INGREDIENT	L35JN3I7SJ	RAMIPRIL TABLET [NORTHWIND PHARMACEUTICALS]	1
RAMIPRILAT	ACTIVE MOIETY	6N5U4QFC3G	RAMIPRIL TABLET [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-117	RAMIPRIL TABLET [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20150126_1a171aaf-e782-4c33-af9b-9806597b1d30.zip