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60512-1007 NDC - BRYONIA ALBA ()

Drug Information

Product NDC: 60512-1007

Proprietary Name: BRYONIA ALBA

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/11/1995

Package Information

No. Package Code Package Description Billing Unit
160512-1007-180 PELLET in 1 TUBE (60512-1007-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC60512-1007The 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 NAMEBRYONIA ALBAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/11/1995This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHOMEOLAB USA 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