Cilag AG
NDC Database

Cilag AG

NDC Database

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

Bulk Ingredient Drug for Further Processing
  • Total Records 7
  • Latest Marketing Date 2021-01-21
  • Data Source FDA
  • First Marketing Date 2010-01-14
All
7
View
Bulk Ingredient
6
View
Drug for Further Processing
1
View
Company Overview

Company

Cilag AG

Country

Switzerland

Website

Visit Website

Email

cilag@its.jnj.com

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Company Snapshot

Cilag AG

Cilag AG Hochstrasse 201 8205 Schaffhausen Switzerland

Switzerland

www.cilag.ch/en/ cilag@its.jnj.com View on Map
NDC Records ( 7 records )
2010
01 Aug
Bulk Ingredient NDC: 12502-4912

Nonproprietary Name

Cladribine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-4912

Substance

CLADRIBINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
14 Jan
Bulk Ingredient NDC: 12502-5263

Nonproprietary Name

Alcaftadine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-5263

Substance

ALCAFTADINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Aug
Bulk Ingredient NDC: 12502-5268

Nonproprietary Name

bortezomib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-5268

Substance

BORTEZOMIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
13 Dec
Bulk Ingredient NDC: 12502-5343

Nonproprietary Name

Remifentanil hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-5343

Substance

REMIFENTANIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2013-12-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Aug
Bulk Ingredient NDC: 12502-5406

Nonproprietary Name

Cladribine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-5406

Substance

CLADRIBINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
21 Jan
Drug for Further Processing NDC: 12502-5500

Nonproprietary Name

rilpivirine hydrochloride

Dosage Form

INJECTION, SUSPENSION

Strength

200 mg/mL

Labeler

Cilag AG

Marketing Category

DRUG FOR FURTHER PROCESSING

12502-5500

Substance

RILPIVIRINE HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2021-01-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
04 Dec
Bulk Ingredient NDC: 12502-6848

Nonproprietary Name

Erdafitinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Cilag AG

Marketing Category

BULK INGREDIENT

12502-6848

Substance

ERDAFITINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
7 total
  • Bulk Ingredient
  • Drug for Further Processing
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 Record Details Preview

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

NDC

12502-4912

Nonproprietary Name

Cladribine

Labeler

Cilag AG

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

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Data maintained from official sources

Structured Database

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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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