Aurolife Pharma LLC Discontinued
FDA Approved Drugs

Aurolife Pharma LLC 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 26
  • Latest Approval Date May 04, 2021
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
74
View
Unclassified
2
View
Discontinued
26
View
OTC
1
View
RX
45
View
Company Overview

Company

Aurolife Pharma LLC Discontinued

Country

U.S.A

Website

Visit Website

Email

achopra@aurobindousa.com

Social Profiles

Company Snapshot

Aurolife Pharma LLC Discontinued

2400 US HWY 130 N Dayton, NJ 08810

U.S.A

www.aurolifepharma.com/ achopra@aurobindousa.com View on Map
FDA Approved Drug Records ( 26 records )
1988
12 Aug
Discontinued Application: 70797

Drug Name

CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

1988-08-12

70797 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

70797

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

1988-08-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80961

Drug Name

CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

80961 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

80961

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
11 May
Discontinued Application: 72514

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1990-05-11

72514 / 1

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72514

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1990-05-11

Regulatory Status

Discontinued

1990
11 May
Discontinued Application: 72514

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

2

Dosage Form

-

Strength

3.75MG

Approval Date

1990-05-11

72514 / 2

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72514

Product Number

2

Dosage Form

-

Strength

3.75MG

Approval Date

1990-05-11

Regulatory Status

Discontinued

1990
11 May
Discontinued Application: 72514

Drug Name

CLORAZEPATE DIPOTASSIUM

Product Number

3

Dosage Form

-

Strength

7.5MG

Approval Date

1990-05-11

72514 / 3

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

72514

Product Number

3

Dosage Form

-

Strength

7.5MG

Approval Date

1990-05-11

Regulatory Status

Discontinued

2013
28 Aug
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2013-08-28

202580 / 1

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2013-08-28

Regulatory Status

Discontinued

2015
25 Aug
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2015-08-25

202580 / 2

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2015-08-25

Regulatory Status

Discontinued

2015
25 Aug
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2015-08-25

202580 / 3

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2015-08-25

Regulatory Status

Discontinued

2015
25 Aug
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2015-08-25

202580 / 4

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2015-08-25

Regulatory Status

Discontinued

2015
21 Dec
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2015-12-21

202580 / 5

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2015-12-21

Regulatory Status

Discontinued

2021
04 May
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

6

Dosage Form

-

Strength

25MG

Approval Date

2021-05-04

202580 / 6

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

6

Dosage Form

-

Strength

25MG

Approval Date

2021-05-04

Regulatory Status

Discontinued

2021
04 May
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

7

Dosage Form

-

Strength

35MG

Approval Date

2021-05-04

202580 / 7

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

7

Dosage Form

-

Strength

35MG

Approval Date

2021-05-04

Regulatory Status

Discontinued

2015
25 Aug
Discontinued Application: 202580

Drug Name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Number

8

Dosage Form

-

Strength

40MG

Approval Date

2015-08-25

202580 / 8

Active Ingredient

DEXMETHYLPHENIDATE HYDROCHLORIDE

Application Number

202580

Product Number

8

Dosage Form

-

Strength

40MG

Approval Date

2015-08-25

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2020-06-24

211876 / 1

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2020-06-24

211876 / 2

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2020-06-24

211876 / 3

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2020-06-24

211876 / 4

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2020-06-24

211876 / 5

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

2020
24 Jun
Discontinued Application: 211876

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2020-06-24

211876 / 6

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

211876

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2020-06-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83899

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83899 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83899

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85219

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85219 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

85219

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2018
25 Oct
Discontinued Application: 209276

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2018-10-25

209276 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

209276

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2018-10-25

Regulatory Status

Discontinued

2018
25 Oct
Discontinued Application: 209276

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2018-10-25

209276 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

209276

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2018-10-25

Regulatory Status

Discontinued

2018
25 Oct
Discontinued Application: 209276

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2018-10-25

209276 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

209276

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2018-10-25

Regulatory Status

Discontinued

2020
27 Jan
Discontinued Application: 212429

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2020-01-27

212429 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

212429

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2020-01-27

Regulatory Status

Discontinued

2020
27 Jan
Discontinued Application: 212429

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG/5ML

Approval Date

2020-01-27

212429 / 2

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

212429

Product Number

2

Dosage Form

-

Strength

100MG/5ML

Approval Date

2020-01-27

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    1 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    74 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
26 total
  • Discontinued
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

CHLORPHENIRAMINE MALEATE

Application Number

70797

Product Number

1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Dosage Form

-

Strength

12MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit