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  5. NDC Package Code: 0703-5003-01 Fluphenazine Decanoate

NDC Package 0703-5003-01 Fluphenazine Decanoate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0703-5003-01
Package Description:
1 VIAL, MULTI-DOSE in 1 CARTON / 5 mL in 1 VIAL, MULTI-DOSE
Product Code:
0703-5003
Proprietary Name:
Fluphenazine Decanoate
Usage Information:
This medication is a long-acting form of fluphenazine that is used to treat certain mental/mood problems (chronic schizophrenia). Fluphenazine decanoate is usually used in patients who have benefited from regular doses of short-acting forms of fluphenazine and who may benefit from long-term (maintenance) treatment with less frequent dosing. Fluphenazine belongs to a class of medications called phenothiazines and is also referred to as a neuroleptic. It works by affecting the balance of natural chemicals (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include reduced episodes of hallucinations, delusions, or bizarre behaviors that occur in patients with schizophrenia. This product does not work right away. It may take 1-3 days to notice an effect from this drug, and up to 4 days to experience the full effect. For severe agitation or other symptoms, use a short-acting medication as directed by your doctor. This medication is not recommended for use in children under 12 years of age. Also, it should not be used to manage behavioral problems in patients with mental retardation.
11-Digit NDC Billing Format:
00703500301
Labeler Name:
Teva Parenteral Medicines, Inc
Sample Package:
No
FDA Application Number:
ANDA074795
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-10-1996
End Marketing Date:
08-29-2005
Listing Expiration Date:
08-29-2005
Exclude Flag:
D
Code Structure:

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.

Frequently Asked Questions

What is NDC 0703-5003-01?

The NDC Packaged Code 0703-5003-01 is assigned to a package of 1 vial, multi-dose in 1 carton / 5 ml in 1 vial, multi-dose of Fluphenazine Decanoate, labeled by Teva Parenteral Medicines, Inc. The product's dosage form is and is administered via form.

Is NDC 0703-5003 included in the NDC Directory?

No, Fluphenazine Decanoate with product code 0703-5003 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Teva Parenteral Medicines, Inc on September 10, 1996 and its listing in the NDC Directory is set to expire on August 29, 2005 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0703-5003-01?

The 11-digit format is 00703500301. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20703-5003-015-4-200703-5003-01