InvaTech Pharma Solutions LLC RX
FDA Approved Drugs

InvaTech Pharma Solutions LLC RX

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 3
  • Latest Approval Date Jul 29, 2008
  • Data Source FDA
  • First Approval Date Jul 29, 2008
All
6
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Discontinued
3
View
RX
3
View
Company Overview

Company

InvaTech Pharma Solutions LLC RX

Country

U.S.A

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Company Snapshot

InvaTech Pharma Solutions LLC RX

40 C Cotters Lane, Suite A, East Brunswick, NJ

U.S.A

inva-tech.com/index.html corporate@inva-tech.com View on Map
FDA Approved Drug Records ( 3 records )
2008
29 Jul
RX Application: 78290

Drug Name

DIVALPROEX SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG VALPROIC ACID

Approval Date

2008-07-29

78290 / 1

Active Ingredient

DIVALPROEX SODIUM

Application Number

78290

Product Number

1

Dosage Form

-

Strength

EQ 500MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

RX

2008
29 Jul
RX Application: 78290

Drug Name

DIVALPROEX SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 250MG VALPROIC ACID

Approval Date

2008-07-29

78290 / 2

Active Ingredient

DIVALPROEX SODIUM

Application Number

78290

Product Number

2

Dosage Form

-

Strength

EQ 250MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

RX

2008
29 Jul
RX Application: 78290

Drug Name

DIVALPROEX SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 125MG VALPROIC ACID

Approval Date

2008-07-29

78290 / 3

Active Ingredient

DIVALPROEX SODIUM

Application Number

78290

Product Number

3

Dosage Form

-

Strength

EQ 125MG VALPROIC ACID

Approval Date

2008-07-29

Regulatory Status

RX

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Drug Status Breakdown
3 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

DIVALPROEX SODIUM

Application Number

78290

Product Number

1

Active Ingredient

DIVALPROEX SODIUM

Dosage Form

-

Strength

EQ 500MG VALPROIC ACID

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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