Bausch Health RX
FDA Approved Drugs

Bausch Health 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 15
  • Latest Approval Date Aug 16, 2002
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
95
View
Unclassified
1
View
Discontinued
79
View
RX
15
View
Company Overview

Company

Bausch Health RX

Country

Canada

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Company Snapshot

Bausch Health RX

2150 St. Elzear Blvd. WestLaval, Quebec H7L 4A8

Canada

www.bauschhealth.com/ View on Map
FDA Approved Drug Records ( 15 records )
1984
26 Oct
RX Application: 50557

Drug Name

BENZAMYCIN

Product Number

1

Dosage Form

-

Strength

5%;3%

Approval Date

1984-10-26

50557 / 1

Active Ingredient

BENZOYL PEROXIDE; ERYTHROMYCIN

Application Number

50557

Product Number

1

Dosage Form

-

Strength

5%;3%

Approval Date

1984-10-26

Regulatory Status

RX

2000
11 Feb
RX Application: 75492

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-02-11

75492 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

75492

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-02-11

Regulatory Status

RX

1999
23 Dec
RX Application: 75116

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1999-12-23

75116 / 1

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

75116

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1999-12-23

Regulatory Status

RX

1999
23 Dec
RX Application: 75116

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

180MG

Approval Date

1999-12-23

75116 / 2

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

75116

Product Number

2

Dosage Form

-

Strength

180MG

Approval Date

1999-12-23

Regulatory Status

RX

1999
23 Dec
RX Application: 75116

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

240MG

Approval Date

1999-12-23

75116 / 3

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

75116

Product Number

3

Dosage Form

-

Strength

240MG

Approval Date

1999-12-23

Regulatory Status

RX

1999
23 Dec
RX Application: 75116

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

300MG

Approval Date

1999-12-23

75116 / 4

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

75116

Product Number

4

Dosage Form

-

Strength

300MG

Approval Date

1999-12-23

Regulatory Status

RX

1982
01 Jan
RX Application: 9170

Drug Name

MYSOLINE

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

9170 / 2

Active Ingredient

PRIMIDONE

Application Number

9170

Product Number

2

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 9170

Drug Name

MYSOLINE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

9170 / 3

Active Ingredient

PRIMIDONE

Application Number

9170

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

RX

2000
04 Dec
RX Application: 75269

Drug Name

NIFEDIPINE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2000-12-04

75269 / 1

Active Ingredient

NIFEDIPINE

Application Number

75269

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2000-12-04

Regulatory Status

RX

2000
04 Dec
RX Application: 75269

Drug Name

NIFEDIPINE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2000-12-04

75269 / 2

Active Ingredient

NIFEDIPINE

Application Number

75269

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2000-12-04

Regulatory Status

RX

2000
27 Sep
RX Application: 75289

Drug Name

NIFEDIPINE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2000-09-27

75289 / 1

Active Ingredient

NIFEDIPINE

Application Number

75289

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2000-09-27

Regulatory Status

RX

2001
06 Feb
RX Application: 75289

Drug Name

NIFEDIPINE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2001-02-06

75289 / 2

Active Ingredient

NIFEDIPINE

Application Number

75289

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2001-02-06

Regulatory Status

RX

2002
16 Aug
RX Application: 76070

Drug Name

NIFEDIPINE

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

2002-08-16

76070 / 1

Active Ingredient

NIFEDIPINE

Application Number

76070

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

2002-08-16

Regulatory Status

RX

2000
31 Aug
RX Application: 21108

Drug Name

RENOVA

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2000-08-31

21108 / 1

Active Ingredient

TRETINOIN

Application Number

21108

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2000-08-31

Regulatory Status

RX

1982
01 Jan
RX Application: 17579

Drug Name

RETIN-A

Product Number

2

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

17579 / 2

Active Ingredient

TRETINOIN

Application Number

17579

Product Number

2

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

RX

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Drug Status Breakdown
15 total
  • RX
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

BENZAMYCIN

Application Number

50557

Product Number

1

Active Ingredient

BENZOYL PEROXIDE; ERYTHROMYCIN

Dosage Form

-

Strength

5%;3%

FDA Approved Drug Data

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