FDA Orange Book

Generic for Periostat

Periostat contains doxycycline. 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 Periostat is doxycycline. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB. Generics match 1 of the 2 Periostat products the Orange Book lists.

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Periostat products in the Orange Book

Periostat products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
capsule, oralEQ 20MG BASEDiscontinuedNone0None
tablet, oralEQ 20MG BASEDiscontinuedNone5AB

NDA 050744, 050783, held by COLLAGENEX INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic doxycycline

Approved generic versions of Periostat
CompanyANDATE codeApprovedStrengths
EPIC PHARMA LLC065182AB (A-rated, therapeutically equivalent)May 13, 2005EQ 20MG BASE
SUN PHARMACEUTICAL INDUSTRIES INC065134AB (A-rated, therapeutically equivalent)May 13, 2005EQ 20MG BASE
CHARTWELL MOLECULAR HOLDINGS LLC065277AB (A-rated, therapeutically equivalent)November 10, 2005EQ 20MG BASE
PHARMOBEDIENT CONSULTING LLC065287AB (A-rated, therapeutically equivalent)February 28, 2006EQ 20MG BASE
ALEMBIC PHARMACEUTICALS LTD210537AB (A-rated, therapeutically equivalent)March 3, 2020EQ 20MG BASE

Questions

Is there a generic for Periostat?

Yes. The generic name for Periostat is doxycycline. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB. Generics match 1 of the 2 Periostat products the Orange Book lists.

What is the generic name for Periostat?

The active ingredient in Periostat is doxycycline, 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.

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