1. Home
  2. Labeler Index
  3. Physicians Total Care, Inc.
  4. NDC Product Code: 54868-1691 Primidone

NDC 54868-1691 Primidone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54868-1691?
  5. Primidone 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:
54868-1691
Proprietary Name:
Primidone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Product Label ID:
c7cb2073-9d44-4261-b308-02cd24c1f17a
Start Marketing Date: [9]
07-27-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
10 MM
Imprint(s):
LAN;1301
LAN;1231
Score:
2

Product Packages

NDC Code 54868-1691-0

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 54868-1691-2

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 54868-1691-3

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 54868-1691-4

Package Description: 10 TABLET in 1 BOTTLE, PLASTIC

NDC Code 54868-1691-5

Package Description: 360 TABLET in 1 BOTTLE

Product Details

What is NDC 54868-1691?

The NDC code 54868-1691 is assigned by the FDA to the product Primidone which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 54868-1691-0 120 tablet in 1 bottle , 54868-1691-2 30 tablet in 1 bottle , 54868-1691-3 100 tablet in 1 bottle , 54868-1691-4 10 tablet in 1 bottle, plastic , 54868-1691-5 360 tablet 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 Primidone?

This medication is used alone or with other medications to control seizures. Controlling and reducing seizures lets you do more of your normal daily activities, reduces your risk of harm when you lose consciousness, and lessens your risk for a possibly life-threatening condition of frequent, repeated seizures. Primidone belongs to a class of drugs known as barbiturate anticonvulsants. It works by controlling the abnormal electrical activity in the brain that occurs during a seizure.

Which are Primidone UNII Codes?

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

Which are Primidone 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 Primidone?

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".