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Orange Book product · Brand (NDA)

OXSORALEN-ULTRA

METHOXSALEN

Brand (NDA)NDA 019600TE ABRX BAUSCH
View METHOXSALEN familyOpen on FDA Orange Book

At a glance

Oct 30, 1986

Approved

Brand (NDA)

Application

AB

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Oct 30, 1986

    40 yr 3 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

METHOXSALEN

Strength

10MG

Dosage form

CAPSULE

Route

ORAL

TE code

AB

Application

NDA 019600

Product number

001

Marketing status

RX

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Active-ingredient family

View full family

This is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

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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