AiPing Pharmaceutical Inc Discontinued
FDA Approved Drugs

AiPing Pharmaceutical Inc 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 55
  • Latest Approval Date Jan 09, 2017
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
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Discontinued
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Company Overview

Company

AiPing Pharmaceutical Inc Discontinued

Country

U.S.A

Website

Visit Website

Email

solutions@aipingpharma.com

Social Profiles

Company Snapshot

AiPing Pharmaceutical Inc Discontinued

350 W Wireless Boulevard\nHauppauge, NY

U.S.A

www.aipingpharmaceutical.com/ solutions@aipingpharma.com View on Map
FDA Approved Drug Records ( 55 records )
2006
21 Dec
Discontinued Application: 76867

Drug Name

ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2006-12-21

76867 / 1

Active Ingredient

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Application Number

76867

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2006-12-21

Regulatory Status

Discontinued

1985
31 Dec
Discontinued Application: 70268

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1985-12-31

70268 / 1

Active Ingredient

ALLOPURINOL

Application Number

70268

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1985-12-31

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2017-01-09

91279 / 1

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2017-01-09

91279 / 2

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2017-01-09

91279 / 3

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2017-01-09

91279 / 4

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2017-01-09

91279 / 5

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 91279

Drug Name

ARIPIPRAZOLE

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

2017-01-09

91279 / 6

Active Ingredient

ARIPIPRAZOLE

Application Number

91279

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

2017-01-09

Regulatory Status

Discontinued

2014
11 Mar
Discontinued Application: 202277

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2014-03-11

202277 / 2

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

202277

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2014-03-11

Regulatory Status

Discontinued

2014
11 Mar
Discontinued Application: 202277

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2014-03-11

202277 / 4

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

202277

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2014-03-11

Regulatory Status

Discontinued

2014
11 Mar
Discontinued Application: 202277

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2014-03-11

202277 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

202277

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2014-03-11

Regulatory Status

Discontinued

2014
11 Mar
Discontinued Application: 202277

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2014-03-11

202277 / 3

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

202277

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2014-03-11

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87381

Drug Name

CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

87381 / 1

Active Ingredient

CHLORTHALIDONE

Application Number

87381

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87381

Drug Name

CHLORTHALIDONE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

87381 / 2

Active Ingredient

CHLORTHALIDONE

Application Number

87381

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1991
19 Nov
Discontinued Application: 72854

Drug Name

CYCLOBENZAPRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1991-11-19

72854 / 1

Active Ingredient

CYCLOBENZAPRINE HYDROCHLORIDE

Application Number

72854

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1991-11-19

Regulatory Status

Discontinued

2006
03 Feb
Discontinued Application: 72854

Drug Name

CYCLOBENZAPRINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2006-02-03

72854 / 2

Active Ingredient

CYCLOBENZAPRINE HYDROCHLORIDE

Application Number

72854

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2006-02-03

Regulatory Status

Discontinued

2011
31 May
Discontinued Application: 90290

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-05-31

90290 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

90290

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-05-31

Regulatory Status

Discontinued

2011
31 May
Discontinued Application: 90290

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2011-05-31

90290 / 2

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

90290

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2011-05-31

Regulatory Status

Discontinued

2011
10 May
Discontinued Application: 91198

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-05-10

91198 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

91198

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-05-10

Regulatory Status

Discontinued

2011
10 May
Discontinued Application: 91198

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2011-05-10

91198 / 2

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

91198

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2011-05-10

Regulatory Status

Discontinued

2012
12 Sep
Discontinued Application: 77512

Drug Name

ESCITALOPRAM OXALATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-09-12

77512 / 1

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

77512

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-09-12

Regulatory Status

Discontinued

2012
12 Sep
Discontinued Application: 77512

Drug Name

ESCITALOPRAM OXALATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-09-12

77512 / 2

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

77512

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-09-12

Regulatory Status

Discontinued

2012
12 Sep
Discontinued Application: 77512

Drug Name

ESCITALOPRAM OXALATE

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2012-09-12

77512 / 3

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

77512

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2012-09-12

Regulatory Status

Discontinued

1987
17 Feb
Discontinued Application: 71128

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1987-02-17

71128 / 1

Active Ingredient

HALOPERIDOL

Application Number

71128

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

1987-02-17

Regulatory Status

Discontinued

1987
17 Feb
Discontinued Application: 71129

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1987-02-17

71129 / 1

Active Ingredient

HALOPERIDOL

Application Number

71129

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1987-02-17

Regulatory Status

Discontinued

1987
12 May
Discontinued Application: 71133

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-05-12

71133 / 1

Active Ingredient

HALOPERIDOL

Application Number

71133

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1987-05-12

Regulatory Status

Discontinued

2009
27 Jan
Discontinued Application: 78645

Drug Name

LAMOTRIGINE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-01-27

78645 / 1

Active Ingredient

LAMOTRIGINE

Application Number

78645

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-01-27

Regulatory Status

Discontinued

2009
27 Jan
Discontinued Application: 78645

Drug Name

LAMOTRIGINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2009-01-27

78645 / 2

Active Ingredient

LAMOTRIGINE

Application Number

78645

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2009-01-27

Regulatory Status

Discontinued

2009
27 Jan
Discontinued Application: 78645

Drug Name

LAMOTRIGINE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2009-01-27

78645 / 3

Active Ingredient

LAMOTRIGINE

Application Number

78645

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2009-01-27

Regulatory Status

Discontinued

2009
27 Jan
Discontinued Application: 78645

Drug Name

LAMOTRIGINE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-01-27

78645 / 4

Active Ingredient

LAMOTRIGINE

Application Number

78645

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-01-27

Regulatory Status

Discontinued

2005
18 Feb
Discontinued Application: 40547

Drug Name

METHIMAZOLE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2005-02-18

40547 / 4

Active Ingredient

METHIMAZOLE

Application Number

40547

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2005-02-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84615

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

84615 / 1

Active Ingredient

METHOCARBAMOL

Application Number

84615

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84616

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84616 / 1

Active Ingredient

METHOCARBAMOL

Application Number

84616

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 91414

Drug Name

MONTELUKAST SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

91414 / 1

Active Ingredient

MONTELUKAST SODIUM

Application Number

91414

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 91414

Drug Name

MONTELUKAST SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

91414 / 2

Active Ingredient

MONTELUKAST SODIUM

Application Number

91414

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80336

Drug Name

PREDNISONE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80336 / 2

Active Ingredient

PREDNISONE

Application Number

80336

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
22 Oct
Discontinued Application: 71288

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

1986-10-22

71288 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

71288

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

1986-10-22

Regulatory Status

Discontinued

1986
13 Nov
Discontinued Application: 70890

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1986-11-13

70890 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70890

Product Number

1

Dosage Form

-

Strength

800MG;160MG

Approval Date

1986-11-13

Regulatory Status

Discontinued

1986
13 Nov
Discontinued Application: 70890

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

2

Dosage Form

-

Strength

400MG;80MG

Approval Date

1986-11-13

70890 / 2

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

70890

Product Number

2

Dosage Form

-

Strength

400MG;80MG

Approval Date

1986-11-13

Regulatory Status

Discontinued

2010
07 Jan
Discontinued Application: 78499

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-01-07

78499 / 1

Active Ingredient

TOPIRAMATE

Application Number

78499

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-01-07

Regulatory Status

Discontinued

2010
07 Jan
Discontinued Application: 78499

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2010-01-07

78499 / 2

Active Ingredient

TOPIRAMATE

Application Number

78499

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2010-01-07

Regulatory Status

Discontinued

2010
07 Jan
Discontinued Application: 78499

Drug Name

TOPIRAMATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2010-01-07

78499 / 3

Active Ingredient

TOPIRAMATE

Application Number

78499

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2010-01-07

Regulatory Status

Discontinued

2010
07 Jan
Discontinued Application: 78499

Drug Name

TOPIRAMATE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2010-01-07

78499 / 4

Active Ingredient

TOPIRAMATE

Application Number

78499

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2010-01-07

Regulatory Status

Discontinued

1990
30 Apr
Discontinued Application: 72483

Drug Name

TRAZODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1990-04-30

72483 / 1

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

72483

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1990-04-30

Regulatory Status

Discontinued

2010
24 May
Discontinued Application: 77478

Drug Name

VALACYCLOVIR HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2010-05-24

77478 / 1

Active Ingredient

VALACYCLOVIR HYDROCHLORIDE

Application Number

77478

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2010-05-24

Regulatory Status

Discontinued

2010
24 May
Discontinued Application: 77478

Drug Name

VALACYCLOVIR HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2010-05-24

77478 / 2

Active Ingredient

VALACYCLOVIR HYDROCHLORIDE

Application Number

77478

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2010-05-24

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2013-06-27

200104 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2013-06-27

200104 / 2

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

2013-06-27

200104 / 3

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2013-06-27

200104 / 4

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

5

Dosage Form

-

Strength

4MG

Approval Date

2013-06-27

200104 / 5

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

5

Dosage Form

-

Strength

4MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

6

Dosage Form

-

Strength

5MG

Approval Date

2013-06-27

200104 / 6

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

6

Dosage Form

-

Strength

5MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

7

Dosage Form

-

Strength

6MG

Approval Date

2013-06-27

200104 / 7

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

7

Dosage Form

-

Strength

6MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

8

Dosage Form

-

Strength

7.5MG

Approval Date

2013-06-27

200104 / 8

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

8

Dosage Form

-

Strength

7.5MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

2013
27 Jun
Discontinued Application: 200104

Drug Name

WARFARIN SODIUM

Product Number

9

Dosage Form

-

Strength

10MG

Approval Date

2013-06-27

200104 / 9

Active Ingredient

WARFARIN SODIUM

Application Number

200104

Product Number

9

Dosage Form

-

Strength

10MG

Approval Date

2013-06-27

Regulatory Status

Discontinued

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Drug Status Breakdown
55 total
  • Discontinued
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

ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Application Number

76867

Product Number

1

Active Ingredient

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

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