Bayer AG Bulk Ingredient
NDC Database
Bayer AG 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 23
- Latest Marketing Date 2024-04-24
- Data Source FDA
- First Marketing Date 2013-04-15
Company Overview
Company
Bayer AG Bulk Ingredient
Country
Germany
Website
Social Profiles
Company Snapshot
Bayer AG Bulk Ingredient
Mullerstr. 178, 13353 Berlin
Germany
pharma.bayer.com/ pharmachemicals@bayer.com View on MapNDC Records ( 23 records )
Nonproprietary Name
Regorafenib Monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
REGORAFENIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-04-24
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Pradofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
PRADOFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-08-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Pradofloxacin Trihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
PRADOFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-08-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Moxifloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
MOXIFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-05-13
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Ciprofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
CIPROFLOXACIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-05-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ciprofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
CIPROFLOXACIN HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-09-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Rivaroxaban Microfine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
RIVAROXABAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-05-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Nifedipine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
NIFEDIPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-10-07
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Enrofloxacin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ENROFLOXACIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-08-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
mesalazin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Estradiol valerate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL VALERATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Testosterone enantate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
TESTOSTERONE ENANTHATE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2017-05-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levonorgestrel
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
LEVONORGESTREL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Norgestrel
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
NORGESTREL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
norethisterone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
NORETHINDRONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Norethisterone acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
NORETHINDRONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ethinylestradiol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ETHINYL ESTRADIOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Estradiol-Hemihydrate Sieved
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL HEMIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Estradiol benzoate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL BENZOATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Medroxyprogesterone acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
MEDROXYPROGESTERONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Ethinylestradiol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ETHINYL ESTRADIOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-10
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Estradiol-Hemihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
ESTRADIOL HEMIHYDRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Tetsoteron Micronized
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Bayer AG
Marketing Category
BULK INGREDIENT
Substance
TESTOSTERONE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2017-05-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
23 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
12527-0181
Nonproprietary Name
Regorafenib Monohydrate
Labeler
Bayer AG
Dosage Form
POWDER
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