Ramipril

Product NDC: 51655-301
11-digit product format: 516550301
Labeler code: 51655
Product ID: 51655-301_9dccd222-84fc-4190-b5fa-2f100d999e2e
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Ramipril
Dosage form: CAPSULE
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA076549
Marketing category: ANDA
Marketing start: 2014-05-07
Marketing end: 0000-00-00
Substance: RAMIPRIL
Active strength: 10 mg/301
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-301-30	2026-01-06	C162847	48780-1	9d75b9d0-7c1e-f424-e053-dadaa90a57ce	2dbd4a0a-09f6-4295-8852-613bd3a0fbfb
51655-301-30	2020-01-31	C162847	48780-1	9d75b9d0-7c1e-f424-e053-dadaa90a57ce	2dbd4a0a-09f6-4295-8852-613bd3a0fbfb

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

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-301	RAMIPRIL CAPSULE [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140520_2dbd4a0a-09f6-4295-8852-613bd3a0fbfb.zip