Vitruvias Therapeutics
FDA Approved Drugs

Vitruvias Therapeutics

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 4
  • Latest Approval Date Feb 06, 2024
  • Data Source FDA
  • First Approval Date Oct 11, 2022
Company Overview

Company

Vitruvias Therapeutics

Country

U.S.A

Social Profiles

Company Snapshot

Vitruvias Therapeutics

778 North Dean Road, Suite 600 Auburn, AL 36830

U.S.A

vitruvias.com/ info@vitruvias.com View on Map
FDA Approved Drug Records ( 4 records )
2022
11 Oct
RX Application: 213985

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

7MG

Approval Date

2022-10-11

213985 / 1

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

213985

Product Number

1

Dosage Form

-

Strength

7MG

Approval Date

2022-10-11

Regulatory Status

RX

2022
11 Oct
RX Application: 213985

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

14MG

Approval Date

2022-10-11

213985 / 2

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

213985

Product Number

2

Dosage Form

-

Strength

14MG

Approval Date

2022-10-11

Regulatory Status

RX

2022
11 Oct
RX Application: 213985

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

28MG

Approval Date

2022-10-11

213985 / 3

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

213985

Product Number

3

Dosage Form

-

Strength

28MG

Approval Date

2022-10-11

Regulatory Status

RX

2024
06 Feb
RX Application: 213985

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

21MG

Approval Date

2024-02-06

213985 / 4

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

213985

Product Number

4

Dosage Form

-

Strength

21MG

Approval Date

2024-02-06

Regulatory Status

RX

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Drug Status Breakdown
4 total
  • RX
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

MEMANTINE HYDROCHLORIDE

Application Number

213985

Product Number

1

Active Ingredient

MEMANTINE HYDROCHLORIDE

Dosage Form

-

Strength

7MG

FDA Approved Drug Data

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