NDC 37808-333-01 Acetaminophen

  1. Labeler Index
  2. H-e-b
  3. 37808-333
  4. NDC Code: 37808-333-01 Acetaminophen

NDC Package Code 37808-333-01

The NDC Code 37808-333-01 is assigned to a package of 100 tablet, extended release in 1 bottle of Acetaminophen, labeled by H-e-b. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 37808-333-01
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
Proprietary Name Acetaminophen 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.
Drug Uses This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format 37808033301 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 H-e-b
Dosage Form -
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 04-30-2002 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 12-31-2019 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. Values = ‘Y’ or ‘N’.
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Code Structure

  • 37808 - H-e-b
    • 37808-333 - Acetaminophen
      • 37808-333-01 - 100 TABLET, EXTENDED RELEASE in 1 BOTTLE

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 Acetaminophen with product NDC 37808-333.

NDC Package CodePackage Description
37808-333-501 BOTTLE in 1 CARTON > 50 TABLET, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.