54575-391 NDC - EGG YOLK ()

Drug Information

Product NDC: 54575-391

Proprietary Name: EGG YOLK

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Allergy Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/29/1972

Package Information

No. Package Code Package Description Billing Unit
154575-391-022 mL in 1 VIAL, MULTI-DOSE (54575-391-02)
254575-391-1010 mL in 1 VIAL, MULTI-DOSE (54575-391-10)
354575-391-3030 mL in 1 VIAL, MULTI-DOSE (54575-391-30)
454575-391-5050 mL in 1 VIAL, MULTI-DOSE (54575-391-50)

NDC Record

Field Name Field Value Definition
PRODUCT NDC54575-391The 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 NAMEEGG YOLKThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/29/1972This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAllergy Laboratories, Inc.Name 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