NDC 0603-6160-32 Trazodone Hydrochloride

Trazodone Hydrochloride

NDC Package Code 0603-6160-32

The NDC Code 0603-6160-32 is assigned to a package of 1000 tablet, film coated in 1 bottle, plastic of Trazodone Hydrochloride, a human prescription drug labeled by Par Pharmaceutical. The product's dosage form is tablet, film coated and is administered via oral form.

Field Name Field Value
NDC Code 0603-6160-32
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Proprietary Name Trazodone Hydrochloride 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 Trazodone Hydrochloride 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 00603616032 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.
Billing Unit EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Product Type Human Prescription Drug 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 Par Pharmaceutical
Dosage Form Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s)
  • Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacological Class(es)
  • Serotonin Reuptake Inhibitor - [EPC] (Established Pharmacologic Class)
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Marketing Category ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number ANDA072192 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Start Marketing Date 05-30-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Start Marketing Date 06-30-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

NDC Code Structure

  • 0603 - Par Pharmaceutical
    • 0603-6160 - Trazodone Hydrochloride
      • 0603-6160-32 - 1000 TABLET, FILM COATED 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.

Pill Identification

Trazodone Hydrochloride 50 MG Oral Tablet

Trazodone Hydrochloride 50 MG Oral Tablet
Image Labeler: Qualitest Pharmaceutical, Inc.

Physical Characteristics

What does trazodone hydrochloride look like?
Trazodone Hydrochloride may look like a white round shaped tablet, film coated; approximately 9 millimeters in size. The medicine is imprinted with debossed code(s) 61 and 60 and V.

Shape: ROUND
Size: 9 mm
Color: WHITE
Imprint: 61;60;V
Imprint Type: DEBOSSED

Other Product Packages

The following packages are also available for Trazodone Hydrochloride with product NDC 0603-6160.

NDC Package CodePackage Description

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