InvaTech Pharma Solutions LLC Discontinued
FDA Approved Drugs

InvaTech Pharma Solutions LLC Discontinued

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.

Discontinued
  • Total Records 3
  • Latest Approval Date Oct 10, 2000
  • Data Source FDA
  • First Approval Date Dec 16, 1982
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Discontinued
3
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RX
3
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Company Overview

Company

InvaTech Pharma Solutions LLC Discontinued

Country

U.S.A

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Company Snapshot

InvaTech Pharma Solutions LLC Discontinued

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 )
2000
10 Oct
Discontinued Application: 75613

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-10-10

75613 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

75613

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-10-10

Regulatory Status

Discontinued

2000
10 Oct
Discontinued Application: 75613

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

75MG

Approval Date

2000-10-10

75613 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

75613

Product Number

2

Dosage Form

-

Strength

75MG

Approval Date

2000-10-10

Regulatory Status

Discontinued

1982
16 Dec
Discontinued Application: 88045

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-12-16

88045 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88045

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-12-16

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • Discontinued
Official Source

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

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

Drug Name

BUPROPION HYDROCHLORIDE

Application Number

75613

Product Number

1

Active Ingredient

BUPROPION HYDROCHLORIDE

Dosage Form

-

Strength

100MG

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