Novartis Pharmaceuticals Corporation
NDC Database
Novartis Pharmaceuticals Corporation
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 80
- Latest Marketing Date 2024-03-14
- Data Source FDA
- First Marketing Date 1983-11-14
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Novartis Pharmaceuticals Corporation
Klybeckstrasse 141, CH-4057, Basel
Switzerland
www.novartis.com/ View on MapNDC Records ( 80 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
letrozole
Dosage Form
TABLET, FILM COATED
Strength
2.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
LETROZOLE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
1997-07-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET, FOR SUSPENSION
Strength
3 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2012-08-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET, FOR SUSPENSION
Strength
5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2012-08-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
trametinib
Dosage Form
TABLET, FILM COATED
Strength
0.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TRAMETINIB DIMETHYL SULFOXIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2016-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
trametinib
Dosage Form
TABLET, FILM COATED
Strength
2 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TRAMETINIB DIMETHYL SULFOXIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2016-03-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
0.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-04-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
0.75 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-04-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
1 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-04-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
asciminib
Dosage Form
TABLET, FILM COATED
Strength
20 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ASCIMINIB HYDROCHLORIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2021-10-29
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
asciminib
Dosage Form
TABLET, FILM COATED
Strength
40 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ASCIMINIB HYDROCHLORIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2021-10-29
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
50 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-05-24
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
siponimod
Dosage Form
TABLET, FILM COATED
Strength
0.25 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SIPONIMOD
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-03-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
siponimod
Dosage Form
TABLET, FILM COATED
Strength
1 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SIPONIMOD
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-03-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
siponimod
Dosage Form
TABLET, FILM COATED
Strength
2 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SIPONIMOD
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-03-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
50 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2022-04-05
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
125 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2022-04-05
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
dabrafenib
Dosage Form
TABLET, FOR SUSPENSION
Strength
10 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
DABRAFENIB MESYLATE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2023-03-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fingolimod hcl
Dosage Form
CAPSULE
Strength
0.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
FINGOLIMOD HYDROCHLORIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-09-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
nilotinib
Dosage Form
CAPSULE
Strength
150 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
NILOTINIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-10-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
nilotinib
Dosage Form
CAPSULE
Strength
200 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
NILOTINIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-10-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
nilotinib
Dosage Form
CAPSULE
Strength
50 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
NILOTINIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-10-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET, FOR SUSPENSION
Strength
2 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2012-08-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
150 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-05-24
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
7.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2011-07-29
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
omalizumab
Dosage Form
INJECTION, SOLUTION
Strength
75 mg/.5mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
OMALIZUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2018-09-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
omalizumab
Dosage Form
INJECTION, SOLUTION
Strength
150 mg/mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
OMALIZUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2018-09-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
omalizumab
Dosage Form
INJECTION, SOLUTION
Strength
300 mg/2mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
OMALIZUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2023-08-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
2.5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-07-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
5 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-03-31
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
10 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-03-31
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
everolimus
Dosage Form
TABLET
Strength
0.25 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
EVEROLIMUS
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2010-04-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
200 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2019-05-24
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
asciminib
Dosage Form
TABLET, FILM COATED
Strength
100 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ASCIMINIB HYDROCHLORIDE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2021-10-29
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
alpelisib
Dosage Form
TABLET
Strength
200 mg/1
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ALPELISIB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2022-04-05
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
canakinumab
Dosage Form
INJECTION, SOLUTION
Strength
150 mg/mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
CANAKINUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2016-12-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
cyclosporine
Dosage Form
INJECTION
Strength
50 mg/mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
CYCLOSPORINE
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
1983-11-14
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
basiliximab
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Strength
10 mg/2.5mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
BASILIXIMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
1998-05-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
tislelizumab-jsgr
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Strength
10 mg/mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
TISLELIZUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2024-03-14
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
omalizumab
Dosage Form
INJECTION, SOLUTION
Strength
150 mg/1.2mL
Labeler
Novartis Pharma Stein AG
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
OMALIZUMAB
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2003-06-20
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
amlodipine besylate and valsartan
Dosage Form
TABLET, FILM COATED
Strength
5; 160 mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
amlodipine valsartan and hydrochlorothiazide
Dosage Form
TABLET, FILM COATED
Strength
5; 12.5; 160 mg/1; mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-04-04
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
amlodipine valsartan and hydrochlorothiazide
Dosage Form
TABLET, FILM COATED
Strength
10; 25; 320 mg/1; mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-04-04
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
amlodipine valsartan and hydrochlorothiazide
Dosage Form
TABLET, FILM COATED
Strength
5; 25; 160 mg/1; mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-04-04
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
amlodipine valsartan and hydrochlorothiazide
Dosage Form
TABLET, FILM COATED
Strength
10; 25; 160 mg/1; mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-04-04
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
amlodipine besylate and valsartan
Dosage Form
TABLET, FILM COATED
Strength
5; 320 mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
amlodipine besylate and valsartan
Dosage Form
TABLET, FILM COATED
Strength
10; 320 mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-06-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Clarithromycin
Dosage Form
PELLET
Strength
400 mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
CLARITHROMYCIN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2007-09-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
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
Somatropin
Dosage Form
INJECTION, SOLUTION
Strength
10 mg/1.5mL
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
SOMATROPIN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2006-05-30
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
amlodipine valsartan and hydrochlorothiazide
Dosage Form
TABLET, FILM COATED
Strength
10; 12.5; 160 mg/1; mg/1; mg/1
Labeler
Novartis Pharmaceuticals Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN
Product Type
HUMAN PRESCRIPTION DRUG
DEA Schedule
Start Marketing Date
2009-04-04
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
80 total- Bulk Ingredient
- Human Prescription Drug
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
44139-0100
Nonproprietary Name
IPTACOPAN
Labeler
Novartis Pharma Schweizerhalle AG
Dosage Form
POWDER
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