Sola Pharmaceuticals
FDA Approved Drugs

Sola Pharmaceuticals

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 6
  • Latest Approval Date Sep 28, 2023
  • Data Source FDA
  • First Approval Date Jun 17, 2020
Company Overview

Company

Sola Pharmaceuticals

Country

U.S.A

Social Profiles

Company Snapshot

Sola Pharmaceuticals

655 Highlandia Dr, Ste B Baton Rouge, LA 70810

U.S.A

www.solameds.us/ info@solameds.us View on Map
FDA Approved Drug Records ( 6 records )
2023
19 May
RX Application: 216824

Drug Name

CARBOPROST TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE/ML

Approval Date

2023-05-19

216824 / 1

Active Ingredient

CARBOPROST TROMETHAMINE

Application Number

216824

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE/ML

Approval Date

2023-05-19

Regulatory Status

RX

2022
15 Apr
RX Application: 215417

Drug Name

CYANOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2022-04-15

215417 / 1

Active Ingredient

CYANOCOBALAMIN

Application Number

215417

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2022-04-15

Regulatory Status

RX

2021
26 Mar
RX Application: 210436

Drug Name

DIMETHYL FUMARATE

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

2021-03-26

210436 / 1

Active Ingredient

DIMETHYL FUMARATE

Application Number

210436

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

2021-03-26

Regulatory Status

RX

2021
26 Mar
RX Application: 210436

Drug Name

DIMETHYL FUMARATE

Product Number

2

Dosage Form

-

Strength

240MG

Approval Date

2021-03-26

210436 / 2

Active Ingredient

DIMETHYL FUMARATE

Application Number

210436

Product Number

2

Dosage Form

-

Strength

240MG

Approval Date

2021-03-26

Regulatory Status

RX

2020
17 Jun
RX Application: 209677

Drug Name

TERIFLUNOMIDE

Product Number

1

Dosage Form

-

Strength

14MG

Approval Date

2020-06-17

209677 / 1

Active Ingredient

TERIFLUNOMIDE

Application Number

209677

Product Number

1

Dosage Form

-

Strength

14MG

Approval Date

2020-06-17

Regulatory Status

RX

2023
28 Sep
RX Application: 209677

Drug Name

TERIFLUNOMIDE

Product Number

2

Dosage Form

-

Strength

7MG

Approval Date

2023-09-28

209677 / 2

Active Ingredient

TERIFLUNOMIDE

Application Number

209677

Product Number

2

Dosage Form

-

Strength

7MG

Approval Date

2023-09-28

Regulatory Status

RX

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Drug Status Breakdown
6 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

CARBOPROST TROMETHAMINE

Application Number

216824

Product Number

1

Active Ingredient

CARBOPROST TROMETHAMINE

Dosage Form

-

Strength

EQ 0.25MG BASE/ML

FDA Approved Drug Data

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