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Orange Book product · Generic (ANDA)

NALOXONE HYDROCHLORIDE

NALOXONE HYDROCHLORIDE

Generic (ANDA)ANDA 213209TE APRX DR REDDYS
View NALOXONE HYDROCHLORIDE familyOpen on FDA Orange Book

At a glance

Mar 16, 2020

Approved

Generic (ANDA)

Application

AP

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Mar 16, 2020

    6 yr 4 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

NALOXONE HYDROCHLORIDE

Strength

1MG/ML

Dosage form

INJECTABLE

Route

INJECTION

TE code

AP

Application

ANDA 213209

Product number

001

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of NALOXONE 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.

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