Cerbios-Pharma SA
NDC Database

Cerbios-Pharma SA

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 9
  • Latest Marketing Date 2016-06-28
  • Data Source FDA
  • First Marketing Date 1983-06-01
Company Overview

Company

Cerbios-Pharma SA

Country

Switzerland

Social Profiles

LinkedIn
Company Snapshot

Cerbios-Pharma SA

Via Figino 6 CH-6917 Barbengo – Lugano

Switzerland

cerbios.swiss/ sales@cerbios.ch View on Map
NDC Records ( 9 records )
1983
01 Jun
Bulk Ingredient NDC: 54239-002

Nonproprietary Name

Leucovorin Calcium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-002

Substance

LEUCOVORIN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1983-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Feb
Bulk Ingredient NDC: 54239-004

Nonproprietary Name

Calcitriol

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-004

Substance

CALCITRIOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
01 Sep
Bulk Ingredient NDC: 54239-005

Nonproprietary Name

Calcipotriene

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-005

Substance

CALCIPOTRIENE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Jan
Bulk Ingredient NDC: 54239-007

Nonproprietary Name

Levoleucovorin Calcium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-007

Substance

LEVOLEUCOVORIN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
01 Jan
Bulk Ingredient NDC: 54239-008

Nonproprietary Name

Levomefolate Calcium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-008

Substance

LEVOMEFOLATE CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jun
Bulk Ingredient NDC: 54239-010

Nonproprietary Name

Doxercalciferol

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-010

Substance

DOXERCALCIFEROL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Oct
Bulk Ingredient NDC: 54239-011

Nonproprietary Name

Tiotropium Bromide

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-011

Substance

TIOTROPIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
19 Jan
Bulk Ingredient NDC: 54239-014

Nonproprietary Name

Levofolinic Acid Crystalline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-014

Substance

LEVOLEUCOVORIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
28 Jun
Bulk Ingredient NDC: 54239-015

Nonproprietary Name

Calcipotriene Monohydrate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cerbios-Pharma SA

Marketing Category

BULK INGREDIENT

54239-015

Substance

CALCIPOTRIENE HYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-06-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 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 Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

54239-002

Nonproprietary Name

Leucovorin Calcium

Labeler

Cerbios-Pharma SA

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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