Altaire Pharmaceuticals Inc.
FDA Approved Drugs

Altaire Pharmaceuticals Inc.

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 OTC
  • Total Records 5
  • Latest Approval Date May 03, 2018
  • Data Source FDA
  • First Approval Date Sep 27, 2010
All
5
View
OTC
1
View
RX
4
View
Company Overview

Company

Altaire Pharmaceuticals Inc.

Country

U.S.A

Website

Email

Social Profiles

Company Snapshot

Altaire Pharmaceuticals Inc.

C/O Teresa Sawaya 91-1 Colin Drive Holbrook, New York 11741

U.S.A

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FDA Approved Drug Records ( 5 records )
2017
14 Dec
RX Application: 208582

Drug Name

ALTAFLUOR BENOX

Product Number

1

Dosage Form

-

Strength

0.4%;0.25%

Approval Date

2017-12-14

208582 / 1

Active Ingredient

BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM

Application Number

208582

Product Number

1

Dosage Form

-

Strength

0.4%;0.25%

Approval Date

2017-12-14

Regulatory Status

RX

2018
03 May
RX Application: 204613

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

2018-05-03

204613 / 1

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

204613

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

2018-05-03

Regulatory Status

RX

2015
16 Nov
RX Application: 203383

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2015-11-16

203383 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

203383

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2015-11-16

Regulatory Status

RX

2010
27 Sep
OTC Application: 78208

Drug Name

NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

0.02675%;0.315%

Approval Date

2010-09-27

78208 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

Application Number

78208

Product Number

1

Dosage Form

-

Strength

0.02675%;0.315%

Approval Date

2010-09-27

Regulatory Status

OTC

2013
29 Apr
RX Application: 202692

Drug Name

OFLOXACIN

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2013-04-29

202692 / 1

Active Ingredient

OFLOXACIN

Application Number

202692

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2013-04-29

Regulatory Status

RX

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  • FDA Approved Drugs Database
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Drug Status Breakdown
5 total
  • RX
  • OTC
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

ALTAFLUOR BENOX

Application Number

208582

Product Number

1

Active Ingredient

BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM

Dosage Form

-

Strength

0.4%;0.25%

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