66594-321 NDC - PRO-CHLO ()

Drug Information

Product NDC: 66594-321

Proprietary Name: PRO-CHLO

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Pro-Pharma, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/12/2011

Package Information

No. Package Code Package Description Billing Unit
166594-321-0130 mL in 1 BOTTLE (66594-321-01)
266594-321-16473 mL in 1 BOTTLE (66594-321-16)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC66594-321The 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 NAMEPRO-CHLOThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/12/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPro-Pharma, 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