Hydrochlorothiazide

Product NDC: 51655-126
11-digit product format: 516550126
Labeler code: 51655
Product ID: 51655-126_0ad79730-c47e-49b0-b9f2-c1766b19c741
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Hydrochlorothiazide
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA040807
Marketing category: ANDA
Marketing start: 2014-08-21
Marketing end: 0000-00-00
Substance: HYDROCHLOROTHIAZIDE
Active strength: 25 mg/1
Pharmacologic classes: Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
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
51655-126-24	2026-01-16	C162847	48780-1	9d75b9cf-efd5-f424-e053-dadaa90a57ce	02ded46d-c8f6-4396-ad70-2ed2a74cbcfd
51655-126-24	2020-01-31	C162847	48780-1	9d75b9cf-efd5-f424-e053-dadaa90a57ce	02ded46d-c8f6-4396-ad70-2ed2a74cbcfd

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
HYDROCHLOROTHIAZIDE	ACTIVE INGREDIENT	0J48LPH2TH	HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
HYDROCHLOROTHIAZIDE	ACTIVE MOIETY	0J48LPH2TH	HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-126	HYDROCHLOROTHIAZIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20140903_02ded46d-c8f6-4396-ad70-2ed2a74cbcfd.zip