THEPHARMANETWORK LLC RX
FDA Approved Drugs

THEPHARMANETWORK 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 9
  • Latest Approval Date Sep 22, 2020
  • Data Source FDA
  • First Approval Date Dec 23, 1985
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Unclassified
2
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RX
9
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Company

THEPHARMANETWORK LLC RX

Country

U.S.A

Website

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Company Snapshot

THEPHARMANETWORK LLC RX

U.S.A

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FDA Approved Drug Records ( 9 records )
2007
30 Mar
RX Application: 40627

Drug Name

BENZONATATE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-03-30

40627 / 1

Active Ingredient

BENZONATATE

Application Number

40627

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-03-30

Regulatory Status

RX

2007
25 Jul
RX Application: 40627

Drug Name

BENZONATATE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-07-25

40627 / 2

Active Ingredient

BENZONATATE

Application Number

40627

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-07-25

Regulatory Status

RX

2014
24 Sep
RX Application: 40627

Drug Name

BENZONATATE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2014-09-24

40627 / 3

Active Ingredient

BENZONATATE

Application Number

40627

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2014-09-24

Regulatory Status

RX

2014
29 Oct
RX Application: 202610

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2014-10-29

202610 / 1

Active Ingredient

ISONIAZID

Application Number

202610

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2014-10-29

Regulatory Status

RX

2014
29 Oct
RX Application: 202610

Drug Name

ISONIAZID

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2014-10-29

202610 / 2

Active Ingredient

ISONIAZID

Application Number

202610

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2014-10-29

Regulatory Status

RX

2009
25 Nov
RX Application: 90635

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2009-11-25

90635 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

90635

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2009-11-25

Regulatory Status

RX

2020
22 Sep
RX Application: 90635

Drug Name

METHADONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2020-09-22

90635 / 2

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

90635

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2020-09-22

Regulatory Status

RX

2014
07 Apr
RX Application: 90103

Drug Name

NIMODIPINE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2014-04-07

90103 / 1

Active Ingredient

NIMODIPINE

Application Number

90103

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2014-04-07

Regulatory Status

RX

1985
23 Dec
RX Application: 18810

Drug Name

THERMAZENE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1985-12-23

18810 / 1

Active Ingredient

SILVER SULFADIAZINE

Application Number

18810

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1985-12-23

Regulatory Status

RX

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Drug Status Breakdown
9 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

BENZONATATE

Application Number

40627

Product Number

1

Active Ingredient

BENZONATATE

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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