61357-152 NDC - SANAFITIL TALCO ()

Drug Information

Product NDC: 61357-152

Proprietary Name: Sanafitil Talco

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ZURICH MEDICAL LABS, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/24/1966

Package Information

No. Package Code Package Description Billing Unit
161357-152-011 BOTTLE in 1 CARTON (61357-152-01) / 57 g in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC61357-152The 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 NAMESanafitil TalcoThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/24/1966This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZURICH MEDICAL LABS, 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