Sigma-Aldrich Corporation
NDC Database

Sigma-Aldrich Corporation

NDC Database

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

Drug for Further Processing Bulk Ingredient
  • Total Records 14
  • Latest Marketing Date 2015-04-16
  • Data Source FDA
  • First Marketing Date 1985-12-23
All
14
View
Bulk Ingredient
13
View
Drug for Further Processing
1
View
Company Overview

Company

Sigma-Aldrich Corporation

Country

U.S.A

Website

Visit Website

Email

cssorders@sial.com

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Company Snapshot

Sigma-Aldrich Corporation

3050 Spruce St, St. Louis, MO 63103

U.S.A

www.sigmaaldrich.com/IE/en cssorders@sial.com View on Map
NDC Records ( 14 records )
1986
20 Feb
Drug for Further Processing NDC: 0441-0670

Nonproprietary Name

Palmitic Acid

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

0441-0670

Substance

PALMITIC ACID

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1986-02-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 Sep
Bulk Ingredient NDC: 0441-0726

Nonproprietary Name

Colfosceril Palmitate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-0726

Substance

COLFOSCERIL PALMITATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 Sep
Bulk Ingredient NDC: 0441-0726

Nonproprietary Name

Colfosceril Palmitate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-0726

Substance

COLFOSCERIL PALMITATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1985
23 Dec
Bulk Ingredient NDC: 0441-0904

Nonproprietary Name

Tripalmitin

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-0904

Substance

TRIPALMITIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1985-12-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
19 Oct
Bulk Ingredient NDC: 0441-1521

Nonproprietary Name

Ferumoxytol Drug Substance

Dosage Form

LIQUID

Strength

200 kg/200kg

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-1521

Substance

FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-10-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
24 Sep
Bulk Ingredient NDC: 0441-2770

Nonproprietary Name

Inosine

Dosage Form

POWDER

Strength

3 kg/3kg

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-2770

Substance

INOSINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
16 Apr
Bulk Ingredient NDC: 0441-3642

Nonproprietary Name

Glatiramer Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

0441-3642

Substance

GLATIRAMER ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1995
02 Jan
Bulk Ingredient NDC: 17445-6034

Nonproprietary Name

Urea-13C

Dosage Form

POWDER

Strength

1800 g/1800g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

17445-6034

Substance

UREA C-13

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1995-01-02

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2000
01 Jan
Bulk Ingredient NDC: 58272-192

Nonproprietary Name

Paricalcitol

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-192

Substance

PARICALCITOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
01 Aug
Bulk Ingredient NDC: 58272-198

Nonproprietary Name

Mechlorethamine Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-198

Substance

MECHLORETHAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
01 Oct
Bulk Ingredient NDC: 58272-199

Nonproprietary Name

Bicisate Dihydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-199

Substance

BICISATE DIHYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
01 May
Bulk Ingredient NDC: 58272-200

Nonproprietary Name

Tetrakis(2-methoxyisobutylisocyanide)Copper(I) tetrafluoroborate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-200

Substance

TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
01 May
Bulk Ingredient NDC: 58272-201

Nonproprietary Name

Halofuginone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-201

Substance

HALOFUGINONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
01 Jan
Bulk Ingredient NDC: 58272-202

Nonproprietary Name

Indocyanine Green

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sigma-Aldrich Corporation

Marketing Category

BULK INGREDIENT

58272-202

Substance

INDOCYANINE GREEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
14 total
  • Drug for Further Processing
  • 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

0441-0670

Nonproprietary Name

Palmitic Acid

Labeler

Sigma-Aldrich Corporation

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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