Xellia Pharmaceuticals ApS
NDC Database
Xellia Pharmaceuticals ApS
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 16
- Latest Marketing Date 2020-12-07
- Data Source FDA
- First Marketing Date 1998-09-01
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Xellia Pharmaceuticals ApS
Dalslandsgade 11, 2300 Copenhagen S
Denmark
www.xellia.com/ info.dk@xellia.com View on MapNDC Records ( 16 records )
Nonproprietary Name
Polymyxin B Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
POLYMYXIN B SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Polymyxin B Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
POLYMYXIN B SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-06-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Colistin Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
COLISTIN SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Amphotericin B
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
AMPHOTERICIN B
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vancomycin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
VANCOMYCIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vancomycin Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
VANCOMYCIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tobramycin sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
TOBRAMYCIN SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-09-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tobramycin sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
TOBRAMYCIN SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-09-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Colistimethate sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
COLISTIMETHATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Colistimethate sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
COLISTIMETHATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Polymyxin B Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
POLYMYXIN B SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-06-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Polymyxin B Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
POLYMYXIN B SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bacitracin Zinc
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
BACITRACIN ZINC
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-07-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vancomycin
Dosage Form
POWDER
Strength
7 kg/7kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
VANCOMYCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-06-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
COLISTIMETHATE SODIUM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Xellia Pharmaceuticals ApS
Marketing Category
BULK INGREDIENT
Substance
COLISTIMETHATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-12-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Gramicidin
Dosage Form
POWDER
Strength
1 g/g
Labeler
Xellia Pharmaceuticals Ltd
Marketing Category
BULK INGREDIENT
Substance
GRAMICIDIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-07-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
16 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
45932-0001
Nonproprietary Name
Polymyxin B Sulfate
Labeler
Xellia Pharmaceuticals ApS
Dosage Form
POWDER
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