70556-100 NDC - SODIUM PHENYLACETATE AND SODIUM BENZOATE ()

Drug Information

Product NDC: 70556-100

Proprietary Name: SODIUM PHENYLACETATE and SODIUM BENZOATE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Ailex Pharmaceuticals, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/24/2016

Package Information

No. Package Code Package Description Billing Unit
170556-100-501 VIAL, SINGLE-DOSE in 1 CARTON (70556-100-50) / 50 mL in 1 VIAL, SINGLE-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70556-100The 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 PHENYLACETATE and SODIUM BENZOATEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/24/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAilex Pharmaceuticals, 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