NDC 0052-0602-02 Tice Bcg

Bacillus Calmette-guerin

NDC Package Code 0052-0602-02

Field Name Field Value
NDC Code 0052-0602-02
Package Description 1 VIAL in 1 CARTON > 50 mL in 1 VIAL (0052-0602-01)
Proprietary Name Tice Bcg Additional informationCallout TooltipWhat 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 Bacillus Calmette-guerin Additional informationCallout TooltipWhat 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 00052060202 Additional informationCallout TooltipNDC 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 Additional informationCallout TooltipWhat 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 Organon Usa Inc.
Dosage Form Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
Administration Route(s)
  • Intravesical - Administration within the bladder.
Active Ingredient(s)
  • BACILLUS CALMETTE-GUERIN SUBSTRAIN TICE LIVE ANTIGEN 50 mg/50mL
Pharmacological Class(es)
  • Live Attenuated Bacillus Calmette-Guerin Vaccine - [EPC] (Established Pharmacologic Class)
  • Actively Acquired Immunity - [PE] (Physiologic Effect)
  • Vaccines -
  • Attenuated - [Chemical/Ingredient]
  • BCG Vaccine - [Chemical/Ingredient]
  • Live Attenuated Bacillus Calmette-Guerin Immunotherapy - [EPC] (Established Pharmacologic Class)
  • Increased Macrophage Proliferation - [PE] (Physiologic Effect)
  • Increased Immunologically Active Molecule Activity - [PE] (Physiologic Effect)
Marketing Category BLA - A product marketed under an approved Biologic License Application. Additional informationCallout TooltipWhat 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 BLA102821 Additional informationCallout TooltipWhat 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 08-24-1990 Additional informationCallout TooltipWhat is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

The NDC Code 0052-0602-02 is assigned to Tice Bcg, a human prescription drug labeled by Organon Usa Inc.. The product's dosage form is powder, for suspension and is administered via intravesical form.


Code Structure
  • 0052 - Organon Usa Inc.
    • 0052-0602 - Tice Bcg
      • 0052-0602-02 - 1 VIAL in 1 CARTON

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.

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NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 0052-0602-02 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
0005206020290585Bcg vaccine percut50 MG1111
0005206020290586Bcg vaccine intravesical1 EACH1111
00052060202J9031Bcg live intravesical vac1 EA1111

* Please review the disclaimer below.

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