NDC Package 75907-082-28 Microgestin Fe 1/20

Norethindrone Acetate/ethinyl Estradiol And Ferrous Fumarate Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
75907-082-28
Package Description:
1 BLISTER PACK in 1 PACKET / 1 KIT in 1 BLISTER PACK
Product Code:
Proprietary Name:
Microgestin Fe 1/20
Non-Proprietary Name:
Norethindrone Acetate/ethinyl Estradiol And Ferrous Fumarate
Usage Information:
Microgestin Fe 1/20 is indicated for the prevention of pregnancy in women who elect to use oral contraceptives as a method of contraception.Oral contraceptives are highly effective. Table I lists the typical accidental pregnancy rates for users of combination oral contraceptives and other methods of contraception. The efficacy of these contraceptive methods, except sterilization, depends upon the reliability with which they are used. Correct and consistent use of methods can result in lower failure rates.Adapted from RA Hatcher et al, Reference 7.TABLE ILOWEST EXPECTED AND TYPICAL FAILURE RATES DURING THE FIRST YEAR OFCONTINUOUS USE OF A METHOD% of Women Experiencing an Unintended Pregnancy in the First Year of Continuous UseMethodLowest Expected*Typical**(No contraception)(85)(85)Oral contraceptives3         combined0.1N/A***         progestin only0.5N/A***Diaphragm with spermicidal cream or jelly620Spermicides alone (foam, creams, gels, vaginal suppositories, and vaginal film)626Vaginal Sponge         nulliparous920         parous2040Implant0.050.05Injection: depot medroxyprogesterone acetate0.30.3IUD         progesterone T1.52.0         copper T 380A0.60.8         LNg 200.10.1Condom without spermicides         female521         male314Cervical Cap with spermicidal cream of jelly         nulliparous920         parous2640Periodic abstinence (all methods)1 to 925Withdrawal419Female sterilization0.50.5Male sterilization0.100.15*The authors' best guess of the percentage of women expected to experience an accidental pregnancy among couples who initiate a method (not necessarily for the first time) and who use it consistently and correctly during the first year if they do not stop for any other reason.**This term represents "typical" couples who initiate use of a method (not necessarily for the first time), who experience an accidental pregnancy during the first year if they do not stop use for any other reason.***N/A--Data not available
11-Digit NDC Billing Format:
75907008228
Product Type:
Human Prescription Drug
Labeler Name:
Dr. Reddy's Laboratories Inc.
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
ANDA091454
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
05-01-2024
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
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
75907-082-626 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK

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Frequently Asked Questions

What is NDC 75907-082-28?

The NDC Packaged Code 75907-082-28 is assigned to a package of 1 blister pack in 1 packet / 1 kit in 1 blister pack of Microgestin Fe 1/20, a human prescription drug labeled by Dr. Reddy's Laboratories Inc.. The product's dosage form is kit and is administered via form.

Is NDC 75907-082 included in the NDC Directory?

Yes, Microgestin Fe 1/20 with product code 75907-082 is active and included in the NDC Directory. The product was first marketed by Dr. Reddy's Laboratories Inc. on May 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 75907-082-28?

The 11-digit format is 75907008228. 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
5-3-275907-082-285-4-275907-0082-28