Chlorpromazine Hydrochloride Injection
NDC Package 70771-1779-7

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Chlorpromazine Hydrochloride injection is classified as a

administered via intramuscular route. This formulation utilizes a injection delivery system. Marketed by Zydus Lifesciences Limited, this product is identified by NDC 70771-1779 and is authorized under FDA application ANDA217275.

Identification & Billing

NDC Package Code
70771-1779-7
Package Description
25 VIAL in 1 CARTON / 2 mL in 1 VIAL (70771-1779-1)
Product Code
70771-1779
11-Digit Billing Format
70771177907
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Chlorpromazine Hydrochloride
Non-Proprietary Name
Chlorpromazine Hydrochloride
Substance Name
Chlorpromazine Hydrochloride
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
Intramuscular - Administration within a muscle.
Active Ingredient(s)
CHLORPROMAZINE HYDROCHLORIDE 25 mg/mL
Pharmacologic Class

Regulatory & Marketing

Labeler Name
Zydus Lifesciences Limited
Product Type
Human Prescription Drug
FDA Application #
ANDA217275
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-29-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70771-1779-7 identifies a specific commercial package of 25 vial in 1 carton / 2 ml in 1 vial (70771-1779-1) of Chlorpromazine Hydrochloride, a human prescription drug labeled by Zydus Lifesciences Limited. This injection is formulated for intramuscular use and contains chlorpromazine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Zydus Lifesciences Limited on March 29, 2024. The current certification is valid through December 31, 2026.

How is this Zydus Lifesciences Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70771177907. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
70771-1779-7
11-Digit CMS (5-4-2)
70771-1779-07

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.