Innogenix
FDA Approved Drugs

Innogenix

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 22
  • Latest Approval Date Oct 29, 2024
  • Data Source FDA
  • First Approval Date Oct 22, 1985
Company Overview

Company

Innogenix

Country

U.S.A

Website

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Company Snapshot

Innogenix

8200 New Horizons Blvd. Amityville, NY 11701

U.S.A

www.innogenix.com/ View on Map
FDA Approved Drug Records ( 22 records )
1988
07 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-01-07

71173 / 1

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-01-07

Regulatory Status

RX

1987
02 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1987-01-02

71173 / 2

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1987-01-02

Regulatory Status

RX

1987
02 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

1987-01-02

71173 / 3

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

1987-01-02

Regulatory Status

RX

1987
02 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

1987-01-02

71173 / 4

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

1987-01-02

Regulatory Status

RX

1988
07 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

1988-01-07

71173 / 5

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

1988-01-07

Regulatory Status

RX

1988
07 Jan
RX Application: 71173

Drug Name

HALOPERIDOL

Product Number

6

Dosage Form

-

Strength

20MG

Approval Date

1988-01-07

71173 / 6

Active Ingredient

HALOPERIDOL

Application Number

71173

Product Number

6

Dosage Form

-

Strength

20MG

Approval Date

1988-01-07

Regulatory Status

RX

1999
29 Jul
RX Application: 75215

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1999-07-29

75215 / 1

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75215

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1999-07-29

Regulatory Status

RX

1999
29 Jul
RX Application: 75215

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1999-07-29

75215 / 2

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75215

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1999-07-29

Regulatory Status

RX

1999
29 Jul
RX Application: 75215

Drug Name

LABETALOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1999-07-29

75215 / 3

Active Ingredient

LABETALOL HYDROCHLORIDE

Application Number

75215

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

1999-07-29

Regulatory Status

RX

2021
30 Mar
RX Application: 213827

Drug Name

METOLAZONE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2021-03-30

213827 / 1

Active Ingredient

METOLAZONE

Application Number

213827

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2021-03-30

Regulatory Status

RX

2021
30 Mar
RX Application: 213827

Drug Name

METOLAZONE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2021-03-30

213827 / 2

Active Ingredient

METOLAZONE

Application Number

213827

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2021-03-30

Regulatory Status

RX

2021
30 Mar
RX Application: 213827

Drug Name

METOLAZONE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2021-03-30

213827 / 3

Active Ingredient

METOLAZONE

Application Number

213827

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2021-03-30

Regulatory Status

RX

1986
16 Jul
RX Application: 70772

Drug Name

METRONIDAZOLE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-07-16

70772 / 1

Active Ingredient

METRONIDAZOLE

Application Number

70772

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1986-07-16

Regulatory Status

RX

1986
16 Jul
RX Application: 70772

Drug Name

METRONIDAZOLE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1986-07-16

70772 / 2

Active Ingredient

METRONIDAZOLE

Application Number

70772

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1986-07-16

Regulatory Status

RX

2024
29 Oct
RX Application: 70772

Drug Name

METRONIDAZOLE

Product Number

3

Dosage Form

-

Strength

125MG

Approval Date

2024-10-29

70772 / 3

Active Ingredient

METRONIDAZOLE

Application Number

70772

Product Number

3

Dosage Form

-

Strength

125MG

Approval Date

2024-10-29

Regulatory Status

RX

2004
22 Dec
RX Application: 76963

Drug Name

PILOCARPINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2004-12-22

76963 / 1

Active Ingredient

PILOCARPINE HYDROCHLORIDE

Application Number

76963

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2004-12-22

Regulatory Status

RX

2007
27 Feb
RX Application: 76963

Drug Name

PILOCARPINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2007-02-27

76963 / 2

Active Ingredient

PILOCARPINE HYDROCHLORIDE

Application Number

76963

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2007-02-27

Regulatory Status

RX

1986
04 Aug
RX Application: 70322

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-08-04

70322 / 1

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70322

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

1986-08-04

Regulatory Status

RX

1985
22 Oct
RX Application: 70322

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1985-10-22

70322 / 2

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70322

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1985-10-22

Regulatory Status

RX

1985
22 Oct
RX Application: 70322

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

1985-10-22

70322 / 3

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70322

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

1985-10-22

Regulatory Status

RX

1985
22 Oct
RX Application: 70322

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

1985-10-22

70322 / 4

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70322

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

1985-10-22

Regulatory Status

RX

1986
24 Sep
RX Application: 70322

Drug Name

PROPRANOLOL HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

60MG

Approval Date

1986-09-24

70322 / 5

Active Ingredient

PROPRANOLOL HYDROCHLORIDE

Application Number

70322

Product Number

5

Dosage Form

-

Strength

60MG

Approval Date

1986-09-24

Regulatory Status

RX

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Drug Status Breakdown
22 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

HALOPERIDOL

Application Number

71173

Product Number

1

Active Ingredient

HALOPERIDOL

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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