69877-017 NDC - ASCORBIC ACID ()

Drug Information

Product NDC: 69877-017

Proprietary Name: Ascorbic Acid

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Raw Materials International Overseas LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/2/2015

Package Information

No. Package Code Package Description Billing Unit
169877-017-011 VIAL, DISPENSING in 1 BOX (69877-017-01) / 50 mL in 1 VIAL, DISPENSING

NDC Record

Field Name Field Value Definition
PRODUCT NDC69877-017The 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 NAMEAscorbic AcidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/2/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERaw Materials International Overseas 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