Navinta Discontinued
FDA Approved Drugs

Navinta 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 Nov 24, 2017
  • Data Source FDA
  • First Approval Date Nov 17, 2009
All
26
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Unclassified
1
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Discontinued
3
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RX
22
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Company Overview

Company

Navinta Discontinued

Country

U.S.A

Social Profiles

Company Snapshot

Navinta Discontinued

1499 Lower Ferry Road Ewing, NJ 08618

U.S.A

www.navinta.com/ sales@navinta.com View on Map
FDA Approved Drug Records ( 3 records )
2017
19 Jul
Discontinued Application: 206561

Drug Name

INDOMETHACIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL

Approval Date

2017-07-19

206561 / 1

Active Ingredient

INDOMETHACIN SODIUM

Application Number

206561

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL

Approval Date

2017-07-19

Regulatory Status

Discontinued

2017
24 Nov
Discontinued Application: 206071

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

1GM/10ML (100MG/ML)

Approval Date

2017-11-24

206071 / 1

Active Ingredient

METHOCARBAMOL

Application Number

206071

Product Number

1

Dosage Form

-

Strength

1GM/10ML (100MG/ML)

Approval Date

2017-11-24

Regulatory Status

Discontinued

2009
17 Nov
Discontinued Application: 90125

Drug Name

NICARDIPINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/10ML (2.5MG/ML)

Approval Date

2009-11-17

90125 / 1

Active Ingredient

NICARDIPINE HYDROCHLORIDE

Application Number

90125

Product Number

1

Dosage Form

-

Strength

25MG/10ML (2.5MG/ML)

Approval Date

2009-11-17

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • Discontinued
Official Source

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

Drug Name

INDOMETHACIN SODIUM

Application Number

206561

Product Number

1

Active Ingredient

INDOMETHACIN SODIUM

Dosage Form

-

Strength

EQ 1MG BASE/VIAL

FDA Approved Drug Data

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