VALSARTAN

Product NDC: 51655-652
11-digit product format: 516550652
Labeler code: 51655
Product ID: 51655-652_f1f70579-c064-459a-a886-86a0c0704e6e
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: VALSARTAN
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA077492
Marketing category: ANDA
Marketing start: 2014-11-13
Marketing end: 0000-00-00
Substance: VALSARTAN
Active strength: 80 mg/1
Pharmacologic classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
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
51655-652-52	2026-01-02	C162847	48780-1	9d75b9d0-6691-f424-e053-dadaa90a57ce	4e2fae79-b8e0-4467-a684-871ba46852be
51655-652-52	2020-01-31	C162847	48780-1	9d75b9d0-6691-f424-e053-dadaa90a57ce	4e2fae79-b8e0-4467-a684-871ba46852be

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
VALSARTAN	ACTIVE INGREDIENT	80M03YXJ7I	VALSARTAN TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1
VALSARTAN	ACTIVE MOIETY	80M03YXJ7I	VALSARTAN TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-652	VALSARTAN TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20141114_4e2fae79-b8e0-4467-a684-871ba46852be.zip