Atorvastatin Calcium

Product NDC: 51655-880
11-digit product format: 516550880
Labeler code: 51655
Product ID: 51655-880_79cc2478-50d8-4961-beb1-1f2bcbec5d3d
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Atorvastatin Calcium
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA020702
Marketing category: ANDA
Marketing start: 2014-04-28
Marketing end: 0000-00-00
Substance: ATORVASTATIN CALCIUM
Active strength: 80 mg/301
Pharmacologic classes: HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase 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
51655-880-30	2026-01-13	C162847	48780-1	9d75b9d1-0024-f424-e053-dadaa90a57ce	2881210e-b0d8-44a1-8540-d7cb985b89b9
51655-880-30	2020-01-31	C162847	48780-1	9d75b9d1-0024-f424-e053-dadaa90a57ce	2881210e-b0d8-44a1-8540-d7cb985b89b9

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ATORVASTATIN CALCIUM	ACTIVE INGREDIENT	48A5M73Z4Q	ATORVASTATIN CALCIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1
ATORVASTATIN	ACTIVE MOIETY	A0JWA85V8F	ATORVASTATIN CALCIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-880	ATORVASTATIN CALCIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140429_2881210e-b0d8-44a1-8540-d7cb985b89b9.zip