Finzala Kit
NDC Package 0093-8210-62
Package Information
Finzala (norethindrone acetate and ethinyl estradiol and ferrous fumarate) kits is finzala is indicated for use by females of reproductive age to prevent pregnancy [see Clinical Studies (14)]. This formulation utilizes a kit delivery system. Marketed by Teva Pharmaceuticals Usa, Inc., this product is identified by NDC 0093-8210 and is authorized under FDA application ANDA210087.
Identification & Billing
- RxCUI: 1426288 - norethindrone acetate 1 MG / ethinyl estradiol 20 MCG Chewable Tablet
- RxCUI: 1426288 - ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Chewable Tablet
- RxCUI: 1426288 - ethinyl estradiol 20 MCG / norethindrone acetate 1 MG Chewable Tablet
- RxCUI: 1426600 - {24 (ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Chewable Tablet) / 4 (ferrous fumarate 75 MG Oral Tablet) } Pack
- RxCUI: 1426600 - Eth estra-Noreth Ac 0.02-1 MG (24) Chewable Tablet / Ferr fum 75 MG (4) Oral Tablet 28 Day Pack
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0093 - Teva Pharmaceuticals Usa, Inc.
- 0093-8210 - Finzala
- 0093-8210-62 - 3 POUCH in 1 CARTON / 1 BLISTER PACK in 1 POUCH (0093-8210-28) / 1 KIT in 1 BLISTER PACK * 24 TABLET, CHEWABLE in 1 BLISTER PACK (0093-3476-38) * 4 TABLET in 1 BLISTER PACK (0093-3525-44)
- 0093-8210 - Finzala
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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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0093-8210-62 identifies a specific commercial package of 3 pouch in 1 carton / 1 blister pack in 1 pouch (0093-8210-28) / 1 kit in 1 blister pack * 24 tablet, chewable in 1 blister pack (0093-3476-38) * 4 tablet in 1 blister pack (0093-3525-44) of Finzala, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. This kit is formulated for use and contains 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 Teva Pharmaceuticals Usa, Inc. on August 04, 2022. The current certification is valid through December 31, 2026.
How is this Teva Pharmaceuticals Usa, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00093821062. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. 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:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.