NDC Package 0009-0370-05 Flavored Colestid

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

0009-0370-05

Package Description:

1 BOTTLE in 1 CARTON / 450 g in 1 BOTTLE

Product Code:

0009-0370

Proprietary Name:

Flavored Colestid

Usage Information:

Since no drug is innocuous, strict attention should be paid to the indications and contraindications, particularly when selecting drugs for chronic long-term use.COLESTID Granules and FLAVORED COLESTID Granules are indicated as adjunctive therapy to diet for the reduction of elevated serum total and low-density lipoprotein (LDL) cholesterol in patients with primary hypercholesterolemia (elevated low density lipoproteins [LDL] cholesterol) who do not respond adequately to diet. Generally, COLESTID and FLAVORED COLESTID have no clinically significant effect on serum triglycerides, but with its use triglyceride levels may be raised in some patients.Therapy with lipid-altering agents should be a component of multiple risk factor intervention in those individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Treatment should begin and continue with dietary therapy (see NCEP guidelines). A minimum of six months of intensive dietary therapy and counseling should be carried out prior to initiation of drug therapy. Shorter periods may be considered in patients with severe elevations of LDL-C or with definite CHD.According to the NCEP guidelines, the goal of treatment is to lower LDL-C, and LDL-C is to be used to initiate and assess treatment response. Only if LDL-C levels are not available, should the Total-C be used to monitor therapy. The NCEP treatment guidelines are shown below.LDL-Cholesterolmg/dL (mmol/L)Definite Atherosclerotic DiseaseCoronary heart disease or peripheral vascular disease (including symptomatic carotid artery disease).Two or More Other Risk FactorsOther risk factors for coronary heart disease (CHD) include: age (males: ≥45 years; females: ≥55 years or premature menopause without estrogen replacement therapy); family history of premature CHD; current cigarette smoking; hypertension; confirmed HDL-C <35 mg/dL (0.91 mmol/L); and diabetes mellitus. Subtract one risk factor if HDL-C is ≥60 mg/dL (1.6 mmol/L).Initiation LevelGoalNoNo≥190(≥4.9)<160(<4.1)NoYes≥160(≥4.1)<130(<3.4)YesYes or No≥130(≥3.4)≤100(≤2.6)

11-Digit NDC Billing Format:

00009037005

Billing Unit:

GM - Billing unit of "gram" is used when a product is measured by its weight.

NDC to RxNorm Crosswalk:

450 GM

NDC to RxNorm Crosswalk:

RxCUI: 1048450 - colestipol HCl 5 GM Granules For Oral Suspension
RxCUI: 1048450 - colestipol hydrochloride 5000 MG Granules for Oral Suspension
RxCUI: 1048450 - colestipol hydrochloride 5 GM Granules For Oral Suspension
RxCUI: 1048452 - Colestid 5 GM Granules For Oral Suspension
RxCUI: 1048452 - colestipol hydrochloride 5000 MG Granules for Oral Suspension [Colestid]

Labeler Name:

Pharmacia & Upjohn Company Llc

Sample Package:

FDA Application Number:

NDA017563

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

06-01-1977

End Marketing Date:

04-30-2024

Listing Expiration Date:

04-30-2024

Exclude Flag:

Code Structure:

0009 - Pharmacia & Upjohn Company Llc
- 0009-0370 - Flavored Colestid
  - 0009-0370-05 - 1 BOTTLE in 1 CARTON / 450 g 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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
0009-0370-03	2 CARTON in 1 CARTON / 60 PACKET in 1 CARTON / 7.5 g in 1 PACKET

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0009-0370-05?

The NDC Packaged Code 0009-0370-05 is assigned to a package of 1 bottle in 1 carton / 450 g in 1 bottle of Flavored Colestid, labeled by Pharmacia & Upjohn Company Llc. The product's dosage form is and is administered via form.This product is billed per "GM" gram and contains an estimated amount of 450 billable units per package.

Is NDC 0009-0370 included in the NDC Directory?

No, Flavored Colestid with product code 0009-0370 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Pharmacia & Upjohn Company Llc on June 01, 1977 and its listing in the NDC Directory is set to expire on April 30, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0009-0370-05?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 450.

What is the 11-digit format for NDC 0009-0370-05?

The 11-digit format is 00009037005. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
4-4-2	0009-0370-05	5-4-2	00009-0370-05

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