FDA Orange Book

Generic for Acticlate

Acticlate 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 Acticlate is doxycycline. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Acticlate products in the Orange Book

Acticlate products and approved generics
Form and route	Strength	Brand status	Brand TE	Active generics	Generic TE codes
tablet, oral	EQ 150MG BASE	Marketed (Rx)	AB	5	AB
tablet, oral	EQ 75MG BASE	Marketed (Rx)	AB	5	AB

NDA 205931, held by CHARTWELL RX SCIENCES LLC. 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 Acticlate
Company	ANDA	TE code	Approved	Strengths
DR REDDYS LABORATORIES SA	208765	AB (A-rated, therapeutically equivalent)	June 14, 2017	EQ 150MG BASE, EQ 75MG BASE
LUPIN LTD	208818	AB (A-rated, therapeutically equivalent)	September 27, 2017	EQ 150MG BASE, EQ 75MG BASE
AJANTA PHARMA LTD	211584	AB (A-rated, therapeutically equivalent)	June 1, 2020	EQ 150MG BASE, EQ 75MG BASE
ALEMBIC PHARMACEUTICALS LTD	211744	AB (A-rated, therapeutically equivalent)	June 30, 2020	EQ 150MG BASE, EQ 75MG BASE
EPIC PHARMA LLC	214207	AB (A-rated, therapeutically equivalent)	December 16, 2020	EQ 150MG BASE, EQ 75MG BASE

Acticlate NDC codes

Questions

Is there a generic for Acticlate?

Yes. The generic name for Acticlate is doxycycline. 5 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 Acticlate?

The active ingredient in Acticlate 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.