69263-805 NDC - BSP 0820 ()

Drug Information

Product NDC: 69263-805

Proprietary Name: BSP 0820

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Oaklock, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/13/2020

Package Information

No. Package Code Package Description Billing Unit
169263-805-011 KIT in 1 CARTON (69263-805-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) / 5 mL in 1 VIAL, MULTI-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC69263-805The 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 NAMEBSP 0820The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/13/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOaklock, 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