51293-607 NDC - CHLORDIAZEPOXIDE HYDROCHLORIDE AND CLIDINIUM BROMIDE ()

Drug Information

Product NDC: 51293-607

Proprietary Name: Chlordiazepoxide Hydrochloride and Clidinium Bromide

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ECI Pharmaceuticals, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/4/2011

Package Information

No. Package Code Package Description Billing Unit
151293-607-01100 CAPSULE in 1 BOTTLE (51293-607-01)EA
251293-607-101000 CAPSULE in 1 BOTTLE (51293-607-10)EA
351293-607-66250 CAPSULE in 1 BOTTLE (51293-607-66)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC51293-607The 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 NAMEChlordiazepoxide Hydrochloride and Clidinium BromideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/4/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEECI Pharmaceuticals, 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