Hovione
NDC Database
Hovione
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 48
- Latest Marketing Date 2026-05-13
- Data Source FDA
- First Marketing Date 1986-11-01
Company Overview
Social Profiles
Company Snapshot
Hovione
Sete Casas 2674 – 506 Loures, Portugal
Portugal
www.hovione.com/ hello@hovione.com View on MapNDC Records ( 48 records )
Nonproprietary Name
ISAVUCONAZONIUM SULFATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
ENSIFENTRINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
BULK INGREDIENT
Substance
ENSIFENTRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-06-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tenapanor hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Viseltinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
Substance
VIMSELTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-02-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sarolaner SDD
Dosage Form
POWDER
Strength
25 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SAROLANER
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2016-02-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ALXN2040/HPMCAS Solid Dispersion
Dosage Form
POWDER
Strength
0.8 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
DANICOPAN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2024-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Deutivacaftor spray dried dispersion
Dosage Form
POWDER
Strength
0.8 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
DEUTIVACAFTOR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2024-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ivosidenib solid dispersion intermediate
Dosage Form
POWDER
Strength
0.5 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
IVOSIDENIB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2018-07-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Suzetrigine spay dried dispersion
Dosage Form
POWDER
Strength
0.25 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SUZETRIGINE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2025-01-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tucatinib solid dispersion intermediate
Dosage Form
POWDER
Strength
0.5 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TUCATINIB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2020-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Apalutamide solid dispersion intermediate
Dosage Form
POWDER
Strength
0.25 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
APALUTAMIDE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2018-02-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paltusotine.HCl SDD
Dosage Form
POWDER
Strength
15 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
PALTUSOTINE HYDROCHLORIDE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2025-09-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zongertinib SDD intermediate
Dosage Form
POWDER
Strength
50 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ZONGERTINIB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2025-08-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
QUIZARTINIB DIHYDROCHLORIDE SDD
Dosage Form
POWDER
Strength
12.73 kg/140kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
QUIZARTINIB DIHYDROCHLORIDE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2023-07-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Grazoprevir SD
Dosage Form
POWDER
Strength
30 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
GRAZOPREVIR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2016-01-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Belzutifan Spray Dried Intermediate
Dosage Form
POWDER
Strength
25 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
BELZUTIFAN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2021-08-13
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Doravirine Spray Dried
Dosage Form
POWDER
Strength
20 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
DORAVIRINE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2018-08-30
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Elbasvir SD
Dosage Form
POWDER
Strength
20 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ELBASVIR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2016-01-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ledipasvir SDD 50% w/w
Dosage Form
POWDER
Strength
50 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
LEDIPASVIR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2019-08-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Velpatasvir SDD 50% w/w
Dosage Form
POWDER
Strength
50 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
VELPATASVIR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2016-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Voxilaprevir SDD
Dosage Form
POWDER
Strength
5 kg/10kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
VOXILAPREVIR
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2017-07-18
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Pirtobrutinib SDD
Dosage Form
POWDER
Strength
50 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
PIRTOBRUTINIB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2023-01-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Orforglipron SDD
Dosage Form
POWDER
Strength
30 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ORFORGLIPRON CALCIUM
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2024-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Orforglipron SDD
Dosage Form
POWDER
Strength
30 kg/100kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ORFORGLIPRON CALCIUM
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2024-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DHE Spray Dried Dispersion
Dosage Form
POWDER
Strength
35.6 kg/100kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
DIHYDROERGOTAMINE MESYLATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2025-04-30
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Sonrotoclax (BGB-11417) SDD
Dosage Form
POWDER
Strength
2 kg/10kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SONROTOCLAX
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2026-05-13
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Tobramycin 28mg Inhalation Powder Hard Capsule
Dosage Form
CAPSULE
Strength
28 mg/1
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TOBRAMYCIN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2024-11-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zongertinib Film-Coated Tablets, 60 mg
Dosage Form
TABLET, COATED
Strength
60 mg/1
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ZONGERTINIB
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2025-08-16
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Salmeterol Xinafoate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Betamethasone sodium phosphate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Betamethasone Acetate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Mometasone Furoate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
MOMETASONE FUROATE MONOHYDRATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Halobetasol Propionate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Fluticasone furoate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Fluticasone Propionate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
HYDROCORTISONE ACEPONATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Doxycycline Hyclate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Doxycycline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
HOVIONE FARMACIENCIA SA
Marketing Category
BULK INGREDIENT
Substance
DOXYCYCLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Minocycline Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Minocycline Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione FarmaCiencia SA
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Ivermectin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
Substance
IVERMECTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-07-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Doxycycline Hyclate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Doxycycline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
Substance
DOXYCYCLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ivermectin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
Substance
IVERMECTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-03-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fluticasone Propionate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Fluticasone Furoate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
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
Nonproprietary Name
Salmeterol xinafoate
Dosage Form
POWDER
Strength
1 g/g
Labeler
Hovione PharmaScience Limited
Marketing Category
BULK INGREDIENT
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
NDC Type Breakdown
48 total- Bulk Ingredient
- Drug for Further Processing
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
50909-1703
Nonproprietary Name
ISAVUCONAZONIUM SULFATE
Labeler
HOVIONE FARMACIENCIA SA
Dosage Form
POWDER
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