Fermion Oy
NDC Database
Fermion Oy
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 20
- Latest Marketing Date 2021-02-15
- Data Source FDA
- First Marketing Date 1981-11-19
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Fermion Oy
Koivu-Mankkaan tie 6 A, FI-02200 Espoo
Finland
www.fermion.fi/ fermionSales@fermion.fi View on MapNDC Records ( 20 records )
Nonproprietary Name
nadolol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
NADOLOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1986-04-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MERCAPTOPURINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
MERCAPTOPURINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-01-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
azathioprine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
AZATHIOPRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-06-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
methotrexate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
METHOTREXATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1981-11-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROXYCHLOROQUINE SULFATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
HYDROXYCHLOROQUINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
buspirone hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
BUSPIRONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1994-10-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
diltiazem hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
DILTIAZEM HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-02-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
carbidopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
CARBIDOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
alprazolam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
ALPRAZOLAM
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
1991-04-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dexmedetomidine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
DEXMEDETOMIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-10-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
glipizide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
GLIPIZIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-12-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
flutamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
FLUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-05-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRILACICLIB DIHYDROCHLORIDE DIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
TRILACICLIB DIHYDROCHLORIDE DIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-02-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
tolnaftate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
TOLNAFTATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-04-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
IRINOTECAN HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
IRINOTECAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-06-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
formoterol fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
FORMOTEROL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
propafenone hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-06-29
End Marketing Date
2028-04-22
Listing Record Certified Through
-
Nonproprietary Name
QUETIAPINE FUMARATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
QUETIAPINE FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-02-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CROMOLYN SODIUM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
CROMOLYN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
methotrexate sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Fermion Oy
Marketing Category
BULK INGREDIENT
Substance
METHOTREXATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
20 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
12780-0154
Nonproprietary Name
nadolol
Labeler
Fermion Oy
Dosage Form
POWDER
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