1. Home
  2. Labeler Index
  3. Belcher Pharmaceuticals Llc
  4. NDC Product Code: 62250-710 Chlorzoxazone

NDC 62250-710 Chlorzoxazone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62250-710?
  5. Chlorzoxazone 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 certification is expired.
NDC Product Code:
62250-710
Proprietary Name:
Chlorzoxazone
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Belcher Pharmaceuticals Llc
Labeler Code:
62250
Product Label ID:
fbd65956-3cbd-4bb4-b340-93ee86da6f8a
Start Marketing Date: [9]
02-02-2023
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - A WHITE TO OFF WHITE CAPSULE SHAPED TABLET DEBOSSED "BPL" ON ONE SIDE AND "250" ON THE OTHER SIDE)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Imprint(s):
BPL;250
Score:
1

Code Structure Chart

Product Details

What is NDC 62250-710?

The NDC code 62250-710 is assigned by the FDA to the product Chlorzoxazone which is product labeled by Belcher Pharmaceuticals Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62250-710-13 60 tablet, orally disintegrating 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 Chlorzoxazone?

Chlorzoxazone is used to treat muscle spasms/pain. It is usually used along with rest, physical therapy, and other treatment. It works by helping to relax the muscles.

Which are Chlorzoxazone UNII Codes?

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

Which are Chlorzoxazone 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".