NDC 61919-122-15 Hydroxyzine Hydrochloride

NDC Package Code 61919-122-15

The NDC Code 61919-122-15 is assigned to a package of 15 tablet, film coated in 1 bottle of Hydroxyzine Hydrochloride, labeled by Direct Rx. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 61919-122-15
Package Description 15 TABLET, FILM COATED in 1 BOTTLE
Proprietary Name Hydroxyzine 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.
11-Digit NDC Billing Format 61919012215 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.
RxNorm Crosswalk995258 - RxCUI What is RxNorm?
The RxNorm crosswalk provides a normalized naming system for generic and branded drugs by assigning unique concept identifiers (RxCUI) to each NDC.
Labeler Name Direct Rx
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 01-01-2015 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

  • 61919 - Direct Rx
    • 61919-122 - Hydroxyzine Hydrochloride
      • 61919-122-15 - 15 TABLET, FILM COATED 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.

Pill Identification

Hydroxyzine Hydrochloride 25 MG Oral Tablet

Hydroxyzine Hydrochloride 25 MG Oral Tablet
Image Labeler: Heritage Pharmaceuticals Inc

Physical Characteristics

What does hydroxyzine hydrochloride look like?
Hydroxyzine Hydrochloride may look like a white round shaped ; approximately 8 millimeters in size. The medicine is imprinted with debossed code(s) H and 106.

Shape: ROUND
Size: 8 mm
Color: WHITE
Imprint: H;106
Imprint Type: DEBOSSED

Active and Inactive Ingredients

Active Ingredients: hydroxyzine hydrochloride 25 mg

Inactive Ingredients: lactose monohydrate, silicon dioxide, hypromellose, magnesium stearate, cellulose, microcrystalline, sodium starch glycolate type a potato, stearic acid, polyethylene glycol, polysorbate 80, titanium dioxide

Other Product Packages

The following packages are also available for Hydroxyzine Hydrochloride with product NDC 61919-122.

NDC Package CodePackage Description
61919-122-2020 TABLET, FILM COATED in 1 BOTTLE
61919-122-3030 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.