FDA.reportPublic FDA data

Anastrozole

Product NDC
51655-638
11-digit product format
516550638
Labeler code
51655
Product ID
51655-638_29d3764c-c67b-4505-8f2d-c4949427d1f3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Anastrozole
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA090568
Marketing category
ANDA
Marketing start
2014-11-07
Marketing end
0000-00-00
Substance
ANASTROZOLE
Active strength
1 mg/1
Pharmacologic classes
Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9495fd23-86bb-d8f7-ae78-6dfe2f4dae2dProduct name320210204

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-638-532026-01-08C16284748780-19d75b9cf-e1f5-f424-e053-dadaa90a57ceAnastrozole
51655-638-532020-01-31C16284748780-19d75b9cf-e1f5-f424-e053-dadaa90a57ceAnastrozole

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANASTROZOLEACTIVE INGREDIENT2Z07MYW1AZANASTROZOLE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
ANASTROZOLEACTIVE MOIETY2Z07MYW1AZANASTROZOLE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-638ANASTROZOLE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1Legacy NDC20141110_f40d2bcc-6b44-455c-8c03-001f39bfecd5.zip