NDC Package 52544-630-31 Microgestin Fe

View Billable Units, 11-Digit Format, RxNorm

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:
52544-630-31
Package Description:
3 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Product Code:
Proprietary Name:
Microgestin Fe
Usage Information:
This combination hormone medication is used to prevent pregnancy. It contains 2 hormones: norethindrone (a progestin) and ethinyl estradiol (an estrogen). It works mainly by preventing the release of an egg (ovulation) during your menstrual cycle. It also makes vaginal fluid thicker to help prevent sperm from reaching an egg (fertilization) and changes the lining of the uterus (womb) to prevent attachment of a fertilized egg. If a fertilized egg does not attach to the uterus, it passes out of the body. There is a small amount of iron (ferrous fumarate) in each of the 7 inactive tablets taken during the fourth week. The inactive pills do not contain any hormones. These tablets are meant to keep you in the habit of taking 1 tablet each day and do not have enough iron to treat iron deficiency. Besides preventing pregnancy, birth control pills may make your periods more regular, decrease blood loss and painful periods, decrease your risk of ovarian cysts, and also treat acne. Using this medication does not protect you or your partner against sexually transmitted diseases (such as HIV, gonorrhea, chlamydia).
11-Digit NDC Billing Format:
52544063031
Labeler Name:
Actavis Pharma, Inc.
Sample Package:
No
FDA Application Number:
ANDA075647
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-05-2001
End Marketing Date:
11-30-2015
Listing Expiration Date:
11-30-2015
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
52544-630-286 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52544-630-31?

The NDC Packaged Code 52544-630-31 is assigned to a package of 3 blister pack in 1 carton / 1 kit in 1 blister pack of Microgestin Fe, labeled by Actavis Pharma, Inc.. The product's dosage form is and is administered via form.

Is NDC 52544-630 included in the NDC Directory?

No, Microgestin Fe with product code 52544-630 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Actavis Pharma, Inc. on February 05, 2001 and its listing in the NDC Directory is set to expire on November 30, 2015 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52544-630-31?

The 11-digit format is 52544063031. 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 5-3-2 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
5-3-252544-630-315-4-252544-0630-31