NDC 49288-0146-4 Cattail

NDC Package Code 49288-0146-4

The NDC Code 49288-0146-4 is assigned to a package of 30 ml in 1 vial, multi-dose of Cattail, labeled by Antigen Laboratories, Inc.. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 49288-0146-4
Package Description 30 mL in 1 VIAL, MULTI-DOSE
Proprietary Name Cattail 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 49288014604 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.
RxNorm Crosswalk1006509, 1014734, 1014738, 1014777, 1098458, 1115952, 1232641, 852018, 852117, 852135, 852139, 852220, 852228, 852332, 852346, 852517, 852662, 852676, 852700, 889573, 889671, 898132 and 898407 - RxCUIs 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 Antigen Laboratories, Inc.
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 03-23-1974 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

  • 49288 - Antigen Laboratories, Inc.
    • 49288-0146 - Cattail
      • 49288-0146-4 - 30 mL in 1 VIAL, MULTI-DOSE

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 Cattail with product NDC 49288-0146.

NDC Package CodePackage Description
49288-0146-12 mL in 1 VIAL, MULTI-DOSE
49288-0146-25 mL in 1 VIAL, MULTI-DOSE
49288-0146-310 mL in 1 VIAL, MULTI-DOSE
49288-0146-550 mL in 1 VIAL, MULTI-DOSE

* Please review the disclaimer below.