pravastatin sodium

Product NDC: 51655-073
11-digit product format: 516550073
Labeler code: 51655
Product ID: 51655-073_aeffdfbb-5721-46e1-829f-fd545b9b5864
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: pravastatin sodium
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA076056
Marketing category: ANDA
Marketing start: 2014-11-12
Marketing end: 0000-00-00
Substance: PRAVASTATIN SODIUM
Active strength: 40 mg/1
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
51655-073-52	2023-02-15	C162847	48780-1	9d75b9d0-ea67-f424-e053-dadaa90a57ce	424d26a3-ebc7-40ab-8303-0422cd26b262
51655-073-52	2020-01-31	C162847	48780-1	9d75b9d0-ea67-f424-e053-dadaa90a57ce	424d26a3-ebc7-40ab-8303-0422cd26b262

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
PRAVASTATIN SODIUM	ACTIVE INGREDIENT	3M8608UQ61	PRAVASTATIN SODIUM TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
PRAVASTATIN	ACTIVE MOIETY	KXO2KT9N0G	PRAVASTATIN SODIUM TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-073	PRAVASTATIN SODIUM TABLET [NORTHWIND PHARMACEUTICALS, LLC]	3	Legacy NDC	20240709_424d26a3-ebc7-40ab-8303-0422cd26b262.zip