Hovione Bulk Ingredient
NDC Database

Hovione Bulk Ingredient

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 24
  • Latest Marketing Date 2025-02-14
  • Data Source FDA
  • First Marketing Date 1986-11-01
All
48
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Bulk Ingredient
24
View
Drug for Further Processing
24
View
Company Overview

Company

Hovione Bulk Ingredient

Country

Portugal

Social Profiles

LinkedIn
Company Snapshot

Hovione Bulk Ingredient

Sete Casas 2674 – 506 Loures, Portugal

Portugal

www.hovione.com/ hello@hovione.com View on Map
NDC Records ( 24 records )
2015
06 Mar
Bulk Ingredient NDC: 50909-1703

Nonproprietary Name

ISAVUCONAZONIUM SULFATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

HOVIONE FARMACIENCIA SA

Marketing Category

BULK INGREDIENT

50909-1703

Substance

ISAVUCONAZONIUM SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-03-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
26 Jun
Bulk Ingredient NDC: 50909-1705

Nonproprietary Name

ENSIFENTRINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

HOVIONE FARMACIENCIA SA

Marketing Category

BULK INGREDIENT

50909-1705

Substance

ENSIFENTRINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-06-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Dec
Bulk Ingredient NDC: 50909-1706

Nonproprietary Name

Tenapanor hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-1706

Substance

TENAPANOR HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
14 Feb
Bulk Ingredient NDC: 50909-1707

Nonproprietary Name

Viseltinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-1707

Substance

VIMSELTINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-02-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
22 Jun
Bulk Ingredient NDC: 50909-4102

Nonproprietary Name

Salmeterol Xinafoate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-4102

Substance

SALMETEROL XINAFOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-06-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
01 Nov
Bulk Ingredient NDC: 50909-5102

Nonproprietary Name

Betamethasone sodium phosphate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5102

Substance

BETAMETHASONE SODIUM PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
01 Nov
Bulk Ingredient NDC: 50909-5103

Nonproprietary Name

Betamethasone Acetate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5103

Substance

BETAMETHASONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 May
Bulk Ingredient NDC: 50909-5151

Nonproprietary Name

Mometasone Furoate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5151

Substance

MOMETASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
23 Apr
Bulk Ingredient NDC: 50909-5152

Nonproprietary Name

MOMETASONE FUROATE MONOHYDRATE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5152

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-04-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
06 Nov
Bulk Ingredient NDC: 50909-5157

Nonproprietary Name

Halobetasol Propionate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5157

Substance

HALOBETASOL PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-11-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
31 May
Bulk Ingredient NDC: 50909-5171

Nonproprietary Name

Fluticasone furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5171

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-05-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
01 Dec
Bulk Ingredient NDC: 50909-5175

Nonproprietary Name

Fluticasone Propionate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-5175

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
09 Jul
Bulk Ingredient NDC: 50909-5263

Nonproprietary Name

HYDROCORTISONE ACEPONATE

Dosage Form

POWDER

Strength

1 g/g

Labeler

HOVIONE FARMACIENCIA SA

Marketing Category

BULK INGREDIENT

50909-5263

Substance

HYDROCORTISONE ACEPONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-07-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
10 Oct
Bulk Ingredient NDC: 50909-8105

Nonproprietary Name

Doxycycline Hyclate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

HOVIONE FARMACIENCIA SA

Marketing Category

BULK INGREDIENT

50909-8105

Substance

DOXYCYCLINE HYCLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
30 Jul
Bulk Ingredient NDC: 50909-8106

Nonproprietary Name

Doxycycline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

HOVIONE FARMACIENCIA SA

Marketing Category

BULK INGREDIENT

50909-8106

Substance

DOXYCYCLINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-07-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
07 Jul
Bulk Ingredient NDC: 50909-9101

Nonproprietary Name

Minocycline Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-9101

Substance

MINOCYCLINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1993-07-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
12 Jan
Bulk Ingredient NDC: 50909-9201

Nonproprietary Name

Minocycline Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione FarmaCiencia SA

Marketing Category

BULK INGREDIENT

50909-9201

Substance

MINOCYCLINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-01-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 Jul
Bulk Ingredient NDC: 55018-121

Nonproprietary Name

Ivermectin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-121

Substance

IVERMECTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1987
01 Apr
Bulk Ingredient NDC: 55018-151

Nonproprietary Name

Doxycycline Hyclate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-151

Substance

DOXYCYCLINE HYCLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1987-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1987
01 Mar
Bulk Ingredient NDC: 55018-164

Nonproprietary Name

Doxycycline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-164

Substance

DOXYCYCLINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1987-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
19 Mar
Bulk Ingredient NDC: 55018-221

Nonproprietary Name

Ivermectin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-221

Substance

IVERMECTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-03-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
23 Nov
Bulk Ingredient NDC: 55018-301

Nonproprietary Name

Fluticasone Propionate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-301

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-11-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
31 May
Bulk Ingredient NDC: 55018-302

Nonproprietary Name

Fluticasone Furoate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-302

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-05-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
22 Jun
Bulk Ingredient NDC: 55018-402

Nonproprietary Name

Salmeterol xinafoate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hovione PharmaScience Limited

Marketing Category

BULK INGREDIENT

55018-402

Substance

SALMETEROL XINAFOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-06-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
24 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

50909-1703

Nonproprietary Name

ISAVUCONAZONIUM SULFATE

Labeler

HOVIONE FARMACIENCIA SA

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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