NDC 69267-101-12 Atenolol Scopolamine

  1. Labeler Index
  2. Tps
  3. 69267-101
  4. NDC Code: 69267-101-12 Atenolol Scopolamine

NDC Package Code 69267-101-12

The NDC Code 69267-101-12 is assigned to a package of 303 mg in 1 bottle, plastic of Atenolol Scopolamine, labeled by Tps. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 69267-101-12
Package Description 303 mg in 1 BOTTLE, PLASTIC
Proprietary Name Atenolol Scopolamine What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
11-Digit NDC Billing Format 69267010112 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Labeler Name Tps
Dosage Form -
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 10-01-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2017 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.
Exclude Flag I 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".
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Code Structure

  • 69267 - Tps
    • 69267-101 - Atenolol Scopolamine
      • 69267-101-12 - 303 mg in 1 BOTTLE, PLASTIC

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for Atenolol Scopolamine with product NDC 69267-101.

NDC Package CodePackage Description
69267-101-06151.5 mg in 1 BOTTLE, PLASTIC
69267-101-24606 mg in 1 BOTTLE, PLASTIC
69267-101-481212 mg in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.