1. Home
  2. Labeler Index
  3. Misemer Pharmaceuticals, Inc
  4. NDC Product Code: 0276-0500 Not Applicable

NDC 0276-0500 Not Applicable

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0276-0500?
  5. Not Applicable Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0276-0500
Proprietary Name:
Not Applicable
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Misemer Pharmaceuticals, Inc
Labeler Code:
0276
Product Label ID:
a42fc981-77bc-4c9e-a79d-b821bffb65b4
Start Marketing Date: [9]
09-03-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - LIGHT GREEN OPAQUE CAPSULES)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Imprint(s):
VP302
Score:
4

Code Structure Chart

Product Details

What is NDC 0276-0500?

The NDC code 0276-0500 is assigned by the FDA to the product Not Applicable which is product labeled by Misemer Pharmaceuticals, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0276-0500-10 100 capsule 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 Not Applicable?

Chlordiazepoxide Hydrochloride and Clidinium Bromide is indicated to control emotional and somatic factors in gastrointestinal disorders. Chlordiazepoxide Hydrochloride and Clidinium Bromide may also be used 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.

Which are Not Applicable UNII Codes?

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

Which are Not Applicable 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:

* 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".