Novartis Pharmaceuticals Corporation Bulk Ingredient
NDC Database
Novartis Pharmaceuticals Corporation 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 31
- Latest Marketing Date 2024-03-14
- Data Source FDA
- First Marketing Date 2003-06-20
Company Overview
Company
Novartis Pharmaceuticals Corporation Bulk Ingredient
Country
Switzerland
Website
Social Profiles
Company Snapshot
Novartis Pharmaceuticals Corporation Bulk Ingredient
Klybeckstrasse 141, CH-4057, Basel
Switzerland
www.novartis.com/ View on MapNDC Records ( 31 records )
Nonproprietary Name
IPTACOPAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
IPTACOPAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-12-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
INCLISIRAN
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
INCLISIRAN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-12-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRAMETINIB DIMETHYL SULFOXIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
TRAMETINIB DIMETHYL SULFOXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
fingolimod hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
FINGOLIMOD HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-09-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
asciminib hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
ASCIMINIB HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-10-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
eltrombopag olamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharma Schweizerhalle AG
Marketing Category
BULK INGREDIENT
Substance
ELTROMBOPAG OLAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
SECUKINUMAB
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
SECUKINUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-01-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
adalimumab-adaz
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
ADALIMUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-07-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
omalizumab
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
OMALIZUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2003-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
tocilizumab
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
TOCILIZUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
denosumab
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
DENOSUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ferumoxytol
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-07-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
alpelisib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
ALPELISIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-04-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
atorvastatin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
lithium carbonate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
LITHIUM CARBONATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-02-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
mycophenolate mofetil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
MYCOPHENOLATE MOFETIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-10-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
pimecrolimus
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
PIMECROLIMUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
tacrolimus
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
TACROLIMUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-08-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
EVEROLIMUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-03-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
somatropin
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
SOMATROPIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2006-05-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
pegfilgrastim
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
PEGFILGRASTIM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-11-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
metreleptin
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
METRELEPTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-03-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
filgrastim
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
FILGRASTIM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-02-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
iptacopan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
IPTACOPAN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-12-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
dabrafenib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
DABRAFENIB MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ribociclib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
RIBOCICLIB SUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-03-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
amlodipine besylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
AMLODIPINE BESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
tislelizumab
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
TISLELIZUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-03-14
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
siponimod
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
SIPONIMOD
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-03-26
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
eltrombopag olamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
ELTROMBOPAG OLAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
ofatumumab
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
BULK INGREDIENT
Substance
OFATUMUMAB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-08-20
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
31 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).
Visit FDA NDC DirectoryNDC Record Details Preview
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NDC
44139-0100
Nonproprietary Name
IPTACOPAN
Labeler
Novartis Pharma Schweizerhalle AG
Dosage Form
POWDER
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