FDA Orange Book
Generic for Brevicon 28-day
Brevicon 28-day contains norethindrone and ethinyl estradiol. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.
Source: FDA Orange Book data file dated 2026-10-09. Publisher page
Yes. The generic name for Brevicon 28-day is norethindrone and ethinyl estradiol. 3 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
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Brevicon 28-day products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| tablet, oral-28 | 0.035MG;0.5MG | Discontinued | None | 3 | AB |
NDA 017743, held by ALLERGAN SALES LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic norethindrone and ethinyl estradiol
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| BARR LABORATORIES LLC (AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC) | 072695 | AB (A-rated, therapeutically equivalent) | February 28, 1992 | 0.035MG;0.5MG |
| NOVAST LABORATORIES LTD | 091204 | AB (A-rated, therapeutically equivalent) | March 27, 2012 | 0.035MG;0.5MG |
| AUROBINDO PHARMA LTD | 207055 | AB (A-rated, therapeutically equivalent) | October 21, 2016 | 0.035MG;0.5MG |
Questions
Is there a generic for Brevicon 28-day?
Yes. The generic name for Brevicon 28-day is norethindrone and ethinyl estradiol. 3 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
What is the generic name for Brevicon 28-day?
The active ingredient in Brevicon 28-day is norethindrone and ethinyl estradiol, per the FDA Orange Book.
What does a therapeutic equivalence code mean?
In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.