Teva Pharmaceutical Industries
NDC Database
Teva Pharmaceutical Industries
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 62
- Latest Marketing Date 2024-10-15
- Data Source FDA
- First Marketing Date 2012-01-04
Company Overview
Social Profiles
Company Snapshot
Teva Pharmaceutical Industries
5 Basel St., Petach Tikva Israel, 49131
Israel
www.tevapharm.com/ View on MapNDC Records ( 62 records )
Nonproprietary Name
Ergotamine Tartrate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
ERGOTAMINE TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dihydroergotoxine Mesylate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
ERGOLOID MESYLATES
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-11-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bromocriptine Mesylate Micronize
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
BROMOCRIPTINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cyclosporine
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
CYCLOSPORINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Butorphanol Tartrate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
BUTORPHANOL TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2013-02-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dihydroergotamine mesylate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
DIHYDROERGOTAMINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Buprenorphine Hydrochloride
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2013-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pergolide Mesylate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PERGOLIDE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-09-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cabergoline
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
CABERGOLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-12-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ergonovine Maleate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
ERGONOVINE MALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tacrolimus
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
TACROLIMUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-05-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mycophenolate Mofetil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
TEVA Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
MYCOPHENOLATE MOFETIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-05-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methylergometrine Maleate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
METHYLERGONOVINE MALEATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-06-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Galanthamine Hydrobromide
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
GALANTAMINE HYDROBROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pemetrexed
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PEMETREXED
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pemetrexed
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PEMETREXED
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-08-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pemetrexed
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PEMETREXED
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-08-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Palonosetron Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PALONOSETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Buprenorphine
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2014-02-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bortezomib
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
BORTEZOMIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-09-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paclitaxel Semisynthetic
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PACLITAXEL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RIVAROXABAN
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-01-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Terguride
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
TERGURIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Laropiprant
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
LAROPIPRANT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-08-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fingolimod HCl
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
FINGOLIMOD HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-01-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cabazitaxel
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
CABAZITAXEL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-01-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pralatrexate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PRALATREXATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-03-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dihydro-alpha-ergocriptine mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
DIHYDRO-.ALPHA.-ERGOCRYPTINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-06-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ingenol Mebutate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
INGENOL MEBUTATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-11-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Perampanel
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PERAMPANEL
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2014-04-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dasatinib Monohydrate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
DASATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-03-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Metopimazine
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
METOPIMAZINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dihydroergotamine
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
DIHYDROERGOTAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-03-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rolapitant
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
ROLAPITANT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-07-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vilanterol Trifenatate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
VILANTEROL TRIFENATATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-10-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Obeticholic Acid
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
OBETICHOLIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-12-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fluticasone Furoate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
FLUTICASONE FUROATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-10-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paliperidone Palmitate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
PALIPERIDONE PALMITATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Voclosporin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
VOCLOSPORIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-04-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Selexipag
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Czech Industries s.r.o
Marketing Category
BULK INGREDIENT
Substance
SELEXIPAG
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-09-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tobramycin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
TOBRAMYCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lovastatin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
LOVASTATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Deferoxamine Mesylate
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
DEFEROXAMINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-24
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mupirocin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
MUPIROCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Simvastatin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
SIMVASTATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pravastatin Sodium
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
PRAVASTATIN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ondansetron Hydrochloride
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
ONDANSETRON HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zaleplon
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
ZALEPLON
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2017-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Bicalutamide
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
BICALUTAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ondansetron
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
ONDANSETRON
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lovastatin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
LOVASTATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-01-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tobramycin Micronized
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
TOBRAMYCIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-10-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Simvastatin Micronized
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
SIMVASTATIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mupirocin Calcium
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
MUPIROCIN CALCIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Mycophenolate Sodium
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
MYCOPHENOLATE SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-01-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levodopa
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-04-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levodopa
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fidaxomycin
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
FIDAXOMICIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-06-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sugammadex Sodium
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
SUGAMMADEX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-10-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sapropterin Dihydrochloride
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
SAPROPTERIN DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Midostaurin Amorph
Dosage Form
POWDER
Strength
100 kg/100kg
Labeler
Teva Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
MIDOSTAURIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-11-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Trilaciclib Hemi-Citrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
TEVA Pharmaceutical Works Private Limited Company
Marketing Category
BULK INGREDIENT
Substance
TRILACICLIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-10-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
62 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
47848-001
Nonproprietary Name
Ergotamine Tartrate
Labeler
Teva Czech Industries s.r.o
Dosage Form
POWDER
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