National Drug Code (NDC) Database
Lonza Biologics Tuas Pte. Ltd.
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NDC:
69438-0015
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Nonproprietary Name:
narsoplimab
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
185 mg/mL
-
Substance:
NARSOPLIMAB
-
Start Marketing Date:
2025-12-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Lonza Biologics Tuas Pte.Ltd.
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NDC:
69438-0011
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Nonproprietary Name:
EFGARTIGIMOD ALFA
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Dosage Form:
LIQUID
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
20 mg/mL
-
Substance:
EFGARTIGIMOD ALFA
-
Start Marketing Date:
2023-02-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lonza Biologics, Inc.
-
NDC:
67643-7008
-
Nonproprietary Name:
Tocilizumab
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
198 mg/mL
-
Substance:
TOCILIZUMAB
-
Start Marketing Date:
2010-01-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lonza Biologics, plc
-
NDC:
17504-0012
-
Nonproprietary Name:
EMAPALUMAB 25 mg/ml
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
25 mg/mL
-
Substance:
EMAPALUMAB
-
Start Marketing Date:
2023-06-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lonza Guangzhou Pharmaceutical Ltd.
-
NDC:
40006-041
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Nonproprietary Name:
SV-006 (Fluvoxamine maleate)
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FLUVOXAMINE MALEATE
-
Start Marketing Date:
2019-02-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lonza Tampa LLC
-
NDC:
70277-504
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Nonproprietary Name:
LEVOKETOCONAZOLE
-
Dosage Form:
TABLET
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
150 mg/1
-
Substance:
LEVOKETOCONAZOLE
-
Start Marketing Date:
2021-12-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Lonza, LLC
-
NDC:
69284-002
-
Nonproprietary Name:
Benzethonium Chloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BENZETHONIUM CHLORIDE
-
Start Marketing Date:
2016-02-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
25905-898
-
Nonproprietary Name:
Benzethonium Chloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BENZETHONIUM CHLORIDE
-
Start Marketing Date:
2012-08-20
-
End Marketing Date:
2026-12-31
-
DEA Schedule:
-
Certified Through:
0000-00-00
-
NDC:
83157-3772
-
Nonproprietary Name:
Nivolumab
-
Dosage Form:
INJECTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
NIVOLUMAB
-
Start Marketing Date:
2014-12-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
73301-018
-
Nonproprietary Name:
pegzilarginase-nbln injection
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
2 mg/.4mL
-
Substance:
PEGZILARGINASE
-
Start Marketing Date:
2026-03-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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