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  4. NDC Product Code: 17856-0407 Carbamazepine

NDC 17856-0407 Carbamazepine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 17856-0407?
  5. Carbamazepine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-0407
Proprietary Name:
Carbamazepine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Product Label ID:
572ef850-a13c-436a-8a29-5afd4cf737c7
Start Marketing Date: [9]
12-15-2011
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - GREEN)
Shape:
CAPSULE (C48336)
Size(s):
16 MM
Imprint(s):
S433;100MG
Score:
1

Product Packages

NDC Code 17856-0407-1

Package Description: 100 POUCH in 1 BOX, UNIT-DOSE / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH

Product Details

What is NDC 17856-0407?

The NDC code 17856-0407 is assigned by the FDA to the product Carbamazepine which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 17856-0407-1 100 pouch in 1 box, unit-dose / 1 capsule, extended release in 1 pouch. 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 Carbamazepine?

Carbamazepine is used to prevent and control seizures. This medication is known as an anticonvulsant or anti-epileptic drug. It is also used to relieve certain types of nerve pain (such as trigeminal neuralgia). This medication works by reducing the spread of seizure activity in the brain and restoring the normal balance of nerve activity.

Which are Carbamazepine UNII Codes?

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

Which are Carbamazepine 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 Carbamazepine?

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: 388311 - carBAMazepine 100 MG 12HR Extended Release Oral Capsule
  • RxCUI: 388311 - 12 HR carbamazepine 100 MG Extended Release Oral Capsule
  • RxCUI: 388311 - carbamazepine 100 MG 12 HR Extended Release Oral Capsule

* Please review the disclaimer below.

Patient Education

Carbamazepine


Carbamazepine is used alone or in combination with other medications to control certain types of seizures in people with epilepsy. It is also used to treat trigeminal neuralgia (a condition that causes facial nerve pain). Carbamazepine extended-release capsules (Equetro brand only) are also used to treat episodes of mania (frenzied, abnormally excited or irritated mood) or mixed episodes (symptoms of mania and depression that happen at the same time) in patients with bipolar I disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). Carbamazepine is in a class of medications called anticonvulsants. It works by reducing abnormal electrical activity in the brain.
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* 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".