61919-546 NDC - PRAVASTATIN SODIUM ()

Drug Information

Product NDC: 61919-546

Proprietary Name: PRAVASTATIN SODIUM

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: DirectRX
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/28/2015

Package Information

No. Package Code Package Description Billing Unit
161919-546-9090 TABLET in 1 BOTTLE (61919-546-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC61919-546The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEPRAVASTATIN SODIUMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/28/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDirectRXName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023