73976-3303 NDC - SANTOTIZER PURE I75 ()

Drug Information

Product NDC: 73976-3303

Proprietary Name: SantOtizer Pure I75

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Santolubes LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/18/2020

Package Information

No. Package Code Package Description Billing Unit
173976-3303-13600 mL in 1 PAIL (73976-3303-1)
273976-3303-218000 mL in 1 PAIL (73976-3303-2)
373976-3303-3200000 mL in 1 DRUM (73976-3303-3)
473976-3303-41022000 mL in 1 TANK (73976-3303-4)
573976-3303-5118.294 mL in 1 BOTTLE, SPRAY (73976-3303-5)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73976-3303The 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 NAMESantOtizer Pure I75The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/18/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESantolubes LLCName 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