53808-0765 NDC - PRAVASTATIN SODIUM ()

Drug Information

Product NDC: 53808-0765

Proprietary Name: Pravastatin Sodium

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	State of Florida DOH Central Pharmacy
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	7/1/2009

No.	Package Code	Package Description	Billing Unit
1	53808-0765-1	30 TABLET in 1 BLISTER PACK (53808-0765-1)

Field Name	Field Value	Definition
PRODUCT NDC	53808-0765
PROPRIETARY NAME	Pravastatin Sodium	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	7/1/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	State of Florida DOH Central Pharmacy	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024