71399-1599 NDC - SODIUM SULFACETAMIDE ()

Drug Information

Product NDC: 71399-1599

Proprietary Name: SODIUM SULFACETAMIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Akron Pharma Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/14/2020

Package Information

No. Package Code Package Description Billing Unit
171399-1599-8237 mL in 1 BOTTLE (71399-1599-8)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC71399-1599The 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 NAMESODIUM SULFACETAMIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/14/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAkron Pharma IncName 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