Azithromycin

Product NDC: 51655-897
11-digit product format: 516550897
Labeler code: 51655
Product ID: 51655-897_8e5ee434-4a94-4a61-e053-2995a90aaa9f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Azithromycin
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA065225
Marketing category: ANDA
Marketing start: 2016-11-13
Marketing end: 0000-00-00
Substance: AZITHROMYCIN MONOHYDRATE
Active strength: 250 mg/1
Pharmacologic classes: Macrolide Antimicrobial [EPC],Macrolides [CS]
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
51655-897-87	2026-01-08	C162847	48780-1	ba0f9c33-5012-a910-e053-dadaa90a0b85	8e5f4b2a-e0ba-b058-e053-2a95a90a1ea0
51655-897-87	2021-01-29	C162847	48780-1	ba0f9c33-5012-a910-e053-dadaa90a0b85	8e5f4b2a-e0ba-b058-e053-2a95a90a1ea0

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-897	AZITHROMYCIN TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	14	Legacy NDC	20190724_8e5f4b2a-e0ba-b058-e053-2a95a90a1ea0.zip