Nephron Pharmaceuticals Corporation RX
FDA Approved Drugs

Nephron Pharmaceuticals Corporation 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 17
  • Latest Approval Date Jun 11, 2026
  • Data Source FDA
  • First Approval Date Sep 17, 1997
All
21
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Unclassified
1
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Discontinued
3
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RX
17
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Company Overview

Company

Nephron Pharmaceuticals Corporation RX

Country

U.S.A

Website

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Company Snapshot

Nephron Pharmaceuticals Corporation RX

4121 SW 34th Street Orlando, FL 32811

U.S.A

www.nephronpharm.com/ View on Map
FDA Approved Drug Records ( 17 records )
1997
17 Sep
RX Application: 74880

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

1997-09-17

74880 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

74880

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

1997-09-17

Regulatory Status

RX

2001
26 Jun
RX Application: 75664

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2001-06-26

75664 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

75664

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2001-06-26

Regulatory Status

RX

2004
28 Jun
RX Application: 76355

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2004-06-28

76355 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

76355

Product Number

1

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2004-06-28

Regulatory Status

RX

2010
31 Mar
RX Application: 76355

Drug Name

ALBUTEROL SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2010-03-31

76355 / 2

Active Ingredient

ALBUTEROL SULFATE

Application Number

76355

Product Number

2

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2010-03-31

Regulatory Status

RX

2007
31 Dec
RX Application: 76749

Drug Name

ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2007-12-31

76749 / 1

Active Ingredient

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Application Number

76749

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2007-12-31

Regulatory Status

RX

2009
30 Mar
RX Application: 78202

Drug Name

BUDESONIDE

Product Number

1

Dosage Form

-

Strength

0.25MG/2ML

Approval Date

2009-03-30

78202 / 1

Active Ingredient

BUDESONIDE

Application Number

78202

Product Number

1

Dosage Form

-

Strength

0.25MG/2ML

Approval Date

2009-03-30

Regulatory Status

RX

2009
30 Mar
RX Application: 78202

Drug Name

BUDESONIDE

Product Number

2

Dosage Form

-

Strength

0.5MG/2ML

Approval Date

2009-03-30

78202 / 2

Active Ingredient

BUDESONIDE

Application Number

78202

Product Number

2

Dosage Form

-

Strength

0.5MG/2ML

Approval Date

2009-03-30

Regulatory Status

RX

2001
27 Sep
RX Application: 75562

Drug Name

IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-09-27

75562 / 1

Active Ingredient

IPRATROPIUM BROMIDE

Application Number

75562

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-09-27

Regulatory Status

RX

2020
20 Aug
RX Application: 211445

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2020-08-20

211445 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

211445

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2020-08-20

Regulatory Status

RX

2026
26 May
RX Application: 215217

Drug Name

LEVALBUTEROL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2026-05-26

215217 / 1

Active Ingredient

LEVALBUTEROL HYDROCHLORIDE

Application Number

215217

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2026-05-26

Regulatory Status

RX

2026
26 May
RX Application: 215217

Drug Name

LEVALBUTEROL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2026-05-26

215217 / 2

Active Ingredient

LEVALBUTEROL HYDROCHLORIDE

Application Number

215217

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2026-05-26

Regulatory Status

RX

2026
11 Jun
RX Application: 216272

Drug Name

NOREPINEPHRINE BITARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2026-06-11

216272 / 1

Active Ingredient

NOREPINEPHRINE BITARTRATE

Application Number

216272

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

2026-06-11

Regulatory Status

RX

2020
23 Apr
RX Application: 211968

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

2020-04-23

211968 / 1

Active Ingredient

SODIUM CHLORIDE

Application Number

211968

Product Number

1

Dosage Form

-

Strength

450MG/50ML (9MG/ML)

Approval Date

2020-04-23

Regulatory Status

RX

2020
23 Apr
RX Application: 211968

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

2020-04-23

211968 / 2

Active Ingredient

SODIUM CHLORIDE

Application Number

211968

Product Number

2

Dosage Form

-

Strength

900MG/100ML

Approval Date

2020-04-23

Regulatory Status

RX

2021
10 Feb
RX Application: 211222

Drug Name

STERILE WATER FOR INJECTION

Product Number

1

Dosage Form

-

Strength

100% (5ML)

Approval Date

2021-02-10

211222 / 1

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211222

Product Number

1

Dosage Form

-

Strength

100% (5ML)

Approval Date

2021-02-10

Regulatory Status

RX

2020
17 Mar
RX Application: 213352

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG/4ML (2.5MG/ML)

Approval Date

2020-03-17

213352 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

213352

Product Number

1

Dosage Form

-

Strength

10MG/4ML (2.5MG/ML)

Approval Date

2020-03-17

Regulatory Status

RX

2020
16 Sep
RX Application: 213352

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

5MG/2ML (2.5MG/ML)

Approval Date

2020-09-16

213352 / 2

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

213352

Product Number

2

Dosage Form

-

Strength

5MG/2ML (2.5MG/ML)

Approval Date

2020-09-16

Regulatory Status

RX

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Drug Status Breakdown
17 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

ALBUTEROL SULFATE

Application Number

74880

Product Number

1

Active Ingredient

ALBUTEROL SULFATE

Dosage Form

-

Strength

EQ 0.083% BASE

FDA Approved Drug Data

Approved drug product information

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