Teva Pharmaceutical Industries OTC
FDA Approved Drugs

Teva Pharmaceutical Industries OTC

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.

OTC
  • Total Records 1
  • Latest Approval Date Apr 19, 2019
  • Data Source FDA
  • First Approval Date Apr 19, 2019
All
831
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Unclassified
80
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Discontinued
412
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OTC
1
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RX
338
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Company Overview

Company

Teva Pharmaceutical Industries OTC

Country

Israel

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Company Snapshot

Teva Pharmaceutical Industries OTC

5 Basel St., Petach Tikva Israel, 49131

Israel

www.tevapharm.com/ View on Map
FDA Approved Drug Records ( 1 record )
2019
19 Apr
OTC Application: 209522

Drug Name

NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

4MG/SPRAY

Approval Date

2019-04-19

209522 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE

Application Number

209522

Product Number

1

Dosage Form

-

Strength

4MG/SPRAY

Approval Date

2019-04-19

Regulatory Status

OTC

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Drug Status Breakdown
1 total
  • OTC
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

NALOXONE HYDROCHLORIDE

Application Number

209522

Product Number

1

Active Ingredient

NALOXONE HYDROCHLORIDE

Dosage Form

-

Strength

4MG/SPRAY

FDA Approved Drug Data

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