NDC 71186-006 Chlordiazepoxide Hydrochloride And Clidinium Bromide

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71186-006
Proprietary Name:
Chlordiazepoxide Hydrochloride And Clidinium Bromide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vilvet Pharmaceuticals Inc
Labeler Code:
71186
Start Marketing Date: [9]
05-01-2011
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Imprint(s):
VIP;115
Score:
1

Product Packages

NDC Code 71186-006-35

Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE

Product Details

What is NDC 71186-006?

The NDC code 71186-006 is assigned by the FDA to the product Chlordiazepoxide Hydrochloride And Clidinium Bromide which is product labeled by Vilvet Pharmaceuticals Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71186-006-35 100 capsule, gelatin coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Chlordiazepoxide Hydrochloride And Clidinium Bromide?

INDICATIONS AND USAGEBased on a review of this drug by the National Academy of Sciences – National Research Council and/or other information, FDA has classified the indications as follows:"Possibly" effective: as adjunctive therapy in the treatment of peptic ulcer and in the treatment of the irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis.Final classification of the less-than-effective indications required further investigation.

Which are Chlordiazepoxide Hydrochloride And Clidinium Bromide UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Chlordiazepoxide Hydrochloride And Clidinium Bromide Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Chlordiazepoxide Hydrochloride And Clidinium Bromide?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 889614 - chlordiazePOXIDE HCl 5 MG / clidinium bromide 2.5 MG Oral Capsule
  • RxCUI: 889614 - chlordiazepoxide hydrochloride 5 MG / clidinium bromide 2.5 MG Oral Capsule

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".