Evonik Bulk Ingredient
NDC Database
Evonik Bulk Ingredient
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 17
- Latest Marketing Date 2024-12-13
- Data Source FDA
- First Marketing Date 1968-06-25
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Evonik Bulk Ingredient
Rellinghauser Straße 1-11, Essen, NRW 45128, DE
Germany
healthcare.evonik.com/en healthcare@evonik.com View on MapNDC Records ( 17 records )
Nonproprietary Name
Gemcitabine hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
EXPORT ONLY
Substance
GEMCITABINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Alectinib HCl
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
ALECTINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tadalafil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
TADALAFIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-11-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Duloxetine hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
DULOXETINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-08-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Enzalutamide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
ENZALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tilmicosin Aqueous
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
TILMICOSIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1996-12-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tilmicosin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
TILMICOSIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-03-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tylosin Intermediate
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
TYLOSIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1968-06-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ractopamine hydrochloric acid
Dosage Form
SUSPENSION
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
RACTOPAMINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-12-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lubabegron fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
LUBABEGRON FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-11-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Baloxavir marboxil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
BALOXAVIR MARBOXIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-12-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Linzagolix Choline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
EXPORT ONLY
Substance
LINZAGOLIX CHOLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-06-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MGL-3196
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
RESMETIROM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-03-14
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Vonoprazan Fumarate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Corporation
Marketing Category
BULK INGREDIENT
Substance
VONOPRAZAN FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-11-21
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Lisinopril Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Rexim S.A.S
Marketing Category
BULK INGREDIENT
Substance
LISINOPRIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-LYSINE HYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Rexim S.A.S
Marketing Category
BULK INGREDIENT
Substance
LYSINE MONOHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1980-07-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-PROLINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Evonik Rexim S.A.S
Marketing Category
BULK INGREDIENT
Substance
PROLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-09-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
17 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
62128-0383
Nonproprietary Name
Gemcitabine hydrochloride
Labeler
Evonik Corporation
Dosage Form
POWDER
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