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Orange Book product · Generic (ANDA)

DOXEPIN HYDROCHLORIDE

DOXEPIN HYDROCHLORIDE

Generic (ANDA)ANDA 074721RX LANNETT CO INC
View DOXEPIN HYDROCHLORIDE familyOpen on FDA Orange Book

At a glance

Dec 29, 1998

Approved

Generic (ANDA)

Application

Not listed

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Dec 29, 1998

    27 yr 10 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

DOXEPIN HYDROCHLORIDE

Strength

EQ 10MG BASE/ML

Dosage form

CONCENTRATE

Route

ORAL

TE code

Not listed

Application

ANDA 074721

Product number

001

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

Yes

Active-ingredient family

View full family

Generic (ANDA) of DOXEPIN HYDROCHLORIDE

Listed patents

No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

Agent CTA Background

Your Next Submission Could Take 6+ Fewer Weeks and Cost $250K Less.

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