Viatris Bulk Ingredient
NDC Database
Viatris 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 37
- Latest Marketing Date 2019-07-15
- Data Source FDA
- First Marketing Date 1989-09-06
Company Overview
Company
Viatris Bulk Ingredient
Country
U.S.A
Website
Social Profiles
Company Snapshot
Viatris Bulk Ingredient
Robert J. Coury Global Center 1000 Mylan Blvd. Canonsburg, PA 15317
U.S.A
www.viatris.com/en HRServiceCenter@Viatris.com View on MapNDC Records ( 37 records )
Nonproprietary Name
ATORVASTATIN CALCIUM
Dosage Form
GRANULE
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-05-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PAROXETINE HYDROCHLORIDE (ANHYDROUS)
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
PAROXETINE HYDROCHLORIDE ANHYDROUS
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-24
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
PRAMIPEXOLE DIHYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
BOSENTAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
BOSENTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-24
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
FORMOTEROL FUMARATE DIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
FORMOTEROL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-03-02
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
LENALIDOMIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
LENALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
PROGUANIL HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
PROGUANIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
RASAGILINE MESYLATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
RASAGILINE MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
TIZANIDINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
TIZANIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
FROVATRIPTAN SUCCINATE MONOHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
FROVATRIPTAN SUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
PRASUGREL HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Mylan Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
PRASUGREL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
ROTIGOTINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
ROTIGOTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
FEBUXOSTAT
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
FEBUXOSTAT
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-08-20
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-20
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
FINGOLIMOD HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
FINGOLIMOD HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-19
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
DIMETHYL FUMARATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
DIMETHYL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-18
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
EPINEPHRINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
EPINEPHRINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-18
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
ROFLUMILAST
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
ROFLUMILAST
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-02-20
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
EPINEPHRINE BITARTRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Mylan Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
EPINEPHRINE BITARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-12-10
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
Macitentan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
MACITENTAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-10-09
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
CARVEDILOL PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
MYLAN LABORATORIES LIMITED
Marketing Category
BULK INGREDIENT
Substance
CARVEDILOL PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-10-02
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
Pomalidomide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Mylan Laboratories Limited
Marketing Category
BULK INGREDIENT
Substance
POMALIDOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-07-15
End Marketing Date
2026-12-01
Listing Record Certified Through
-
Nonproprietary Name
celecoxib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Amlodipine Besylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
AMLODIPINE BESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Latanoprost
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
LATANOPROST
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sertraline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
SERTRALINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Varenicline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
VARENICLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Azithromycin Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
AZITHROMYCIN DIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Parecoxib sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
PARECOXIB SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Doxazosin Mesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
DOXAZOSIN MESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Tolterodine Tartrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
TOLTERODINE TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
tolterodine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
TOLTERODINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
fluconazole
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
FLUCONAZOLE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Exemestane
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
EXEMESTANE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
nifedipine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
NIFEDIPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1989-09-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Azithromycin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
AZITHROMYCIN, UNSPECIFIED FORM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-04-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Linezolid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Viatris Pharmaceuticals LLC
Marketing Category
BULK INGREDIENT
Substance
LINEZOLID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
37 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
65015-282
Nonproprietary Name
ATORVASTATIN CALCIUM
Labeler
MYLAN LABORATORIES LIMITED
Dosage Form
GRANULE
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