Ajinomoto Company
NDC Database
Ajinomoto Company
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 25
- Latest Marketing Date 2022-10-01
- Data Source FDA
- First Marketing Date 1982-04-15
Company Overview
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Ajinomoto Company
15-1, Kyobashi 1-chome, Chuo-ku, Tokyo 104-8315
Japan
www.ajinomoto.com/ webmaster@ms.ajinomoto.co.jp View on MapNDC Records ( 25 records )
Nonproprietary Name
Arginine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
ARGININE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Arginine Monohydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
ARGININE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-28
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
ASPARTIC ACID
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
ASPARTIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Glutamic Acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
GLUTAMIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
GLYCINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
GLYCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lysine Monohydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
LYSINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHIONINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
METHIONINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Tyrosine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
TYROSINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-01-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TAURINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
TAURINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
N-ACETYL-L-TYROSINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
ACETYL L-TYROSINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LEVODOPA
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1982-04-15
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
N-Acetyl-DL-Tryptophan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
N-ACETYL-DL-TRYPTOPHAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Cysteine Hydrochloride Monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
CYSTEINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Phenylalanine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Co., Inc.
Marketing Category
BULK INGREDIENT
Substance
PHENYLALANINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Glutamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto do Brasil Industria e Comercio de Alimentos Ltda.
Marketing Category
BULK INGREDIENT
Substance
GLUTAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-10-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
L-ISOLEUCINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto do Brasil Industria e Comercio de Alimentos Ltda.
Marketing Category
BULK INGREDIENT
Substance
ISOLEUCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Isoleucine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto do Brasil Industria e Comercio de Alimentos Ltda.
Marketing Category
BULK INGREDIENT
Substance
ISOLEUCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-10-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Not Applicable
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Omnichem
Marketing Category
BULK INGREDIENT
Substance
CANAGLIFLOZIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-11-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
not applicable
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Omnichem
Marketing Category
BULK INGREDIENT
Substance
GEFITINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-01-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
not applicable
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Ajinomoto Omnichem
Marketing Category
BULK INGREDIENT
Substance
BRIGATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Lysine Monohydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shanghai Ajinomoto Amino Acid Co., Ltd.
Marketing Category
BULK INGREDIENT
Substance
LYSINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Isoleucine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shanghai Ajinomoto Amino Acid Co., Ltd.
Marketing Category
BULK INGREDIENT
Substance
ISOLEUCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-01-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Leucine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shanghai Ajinomoto Amino Acid Co., Ltd.
Marketing Category
BULK INGREDIENT
Substance
LEUCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Phenylalanine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shanghai Ajinomoto Amino Acid Co., Ltd.
Marketing Category
BULK INGREDIENT
Substance
PHENYLALANINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Valine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shanghai Ajinomoto Amino Acid Co., Ltd.
Marketing Category
BULK INGREDIENT
Substance
VALINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-23
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
25 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
17333-002
Nonproprietary Name
Arginine
Labeler
Ajinomoto Co., Inc.
Dosage Form
POWDER
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