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  4. NDC Product Code: 67046-935 Chlordiazepoxide Hydrochloride

NDC 67046-935 Chlordiazepoxide Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67046-935?
  5. Chlordiazepoxide Hydrochloride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67046-935
Proprietary Name:
Chlordiazepoxide Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Contract Pharmacy Services-pa
Labeler Code:
67046
Product Label ID:
58113333-a25e-2cd0-e053-2991aa0a35ef
Start Marketing Date: [9]
05-15-2010
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - GREEN;BLACK)
GREEN (C48329 - GREEN;WHITE)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Imprint(s):
S252;S
S253;S
Score:
1

Product Packages

NDC Code 67046-935-30

Package Description: 30 CAPSULE, GELATIN COATED in 1 BLISTER PACK

Product Details

What is NDC 67046-935?

The NDC code 67046-935 is assigned by the FDA to the product Chlordiazepoxide Hydrochloride which is product labeled by Contract Pharmacy Services-pa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67046-935-30 30 capsule, gelatin coated in 1 blister pack . 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?

Chlordiazepoxide Hydrochloride Capsule is indicated for the management of anxiety disorders or for the short term relief of symptoms of anxiety, withdrawal symptoms of acute alcoholism, and preoperative apprehension and anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic.The effectiveness of Chlordiazepoxide Hydrochloride Capsule in long-term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should periodically reassess the usefulness of the drug for the individual patient.

Which are Chlordiazepoxide Hydrochloride UNII Codes?

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

  • CHLORDIAZEPOXIDE HYDROCHLORIDE (UNII: MFM6K1XWDK)
  • CHLORDIAZEPOXIDE (UNII: 6RZ6XEZ3CR) (Active Moiety)

Which are Chlordiazepoxide Hydrochloride 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?

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:

* 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".