Losatan Potassium

Product NDC: 51655-258
11-digit product format: 516550258
Labeler code: 51655
Product ID: 51655-258_7e7ef586-aebe-bd3d-e053-2a91aa0a3ada
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Losatan Potassium
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA090428
Marketing category: ANDA
Marketing start: 2019-01-02
Marketing end: 0000-00-00
Substance: LOSARTAN POTASSIUM
Active strength: 25 mg/1
Pharmacologic classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-258-30	2026-01-07	C162847	48780-1	ba0f9c33-56eb-a910-e053-dadaa90a0b85	7e7ecbc9-0baa-0cb8-e053-2991aa0a31fa
51655-258-30	2021-01-29	C162847	48780-1	ba0f9c33-56eb-a910-e053-dadaa90a0b85	7e7ecbc9-0baa-0cb8-e053-2991aa0a31fa

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-258	LOSATAN POTASSIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20190103_7e7ecbc9-0baa-0cb8-e053-2991aa0a31fa.zip