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Orange Book product · Generic (ANDA)

MECLOFENAMATE SODIUM

MECLOFENAMATE SODIUM

Generic (ANDA)ANDA 071081RX MYLAN
View MECLOFENAMATE SODIUM familyOpen on FDA Orange Book

At a glance

Sep 03, 1986

Approved

Generic (ANDA)

Application

Not listed

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Sep 03, 1986

    40 yr 4 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

MECLOFENAMATE SODIUM

Strength

EQ 50MG BASE

Dosage form

CAPSULE

Route

ORAL

TE code

Not listed

Application

ANDA 071081

Product number

002

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of MECLOFENAMATE SODIUM

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

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