Oyster Point Pharma
FDA Approved Drugs

Oyster Point Pharma

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX
  • Total Records 1
  • Latest Approval Date Oct 15, 2021
  • Data Source FDA
  • First Approval Date Oct 15, 2021
Company Overview

Company

Oyster Point Pharma

Country

U.S.A

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Oyster Point Pharma

700 Alexander Park Drive, Suite 301 Princeton, New Jersey 08540

U.S.A

oysterpointrx.com/ info@oysterpointrx.com View on Map
FDA Approved Drug Records ( 1 record )
2021
15 Oct
RX Application: 213978

Drug Name

TYRVAYA

Product Number

1

Dosage Form

-

Strength

EQ 0.03MG BASE/SPRAY

Approval Date

2021-10-15

213978 / 1

Active Ingredient

VARENICLINE TARTRATE

Application Number

213978

Product Number

1

Dosage Form

-

Strength

EQ 0.03MG BASE/SPRAY

Approval Date

2021-10-15

Regulatory Status

RX

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Drug Status Breakdown
1 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

TYRVAYA

Application Number

213978

Product Number

1

Active Ingredient

VARENICLINE TARTRATE

Dosage Form

-

Strength

EQ 0.03MG BASE/SPRAY

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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