Strem Chemicals, Inc.
NDC Database

Strem Chemicals, Inc.

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 2023-12-18
  • Data Source FDA
  • First Marketing Date 1995-02-16
Company Overview

Company

Strem Chemicals, Inc.

Country

U.S.A

Website

Visit Website

Email

info@strem.com

Social Profiles

Company Snapshot

Strem Chemicals, Inc.

7 Mulliken Way Newburyport MA 01950

U.S.A

www.strem.com/ info@strem.com View on Map
NDC Records ( 9 records )
2022
12 Dec
Bulk Ingredient NDC: 50711-0013

Nonproprietary Name

Manganese Sulfate

Dosage Form

INJECTION

Strength

1 kg/kg

Labeler

Strem Chemicals, Inc

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0013

Substance

MANGANESE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-12-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1995
16 Feb
Bulk Ingredient NDC: 50711-0001

Nonproprietary Name

Cisplatin

Dosage Form

INJECTION

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0001

Substance

CISPLATIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1995-02-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
25 Nov
Bulk Ingredient NDC: 50711-0003

Nonproprietary Name

Pamidronic Acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT

50711-0003

Substance

PAMIDRONIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-11-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
21 Mar
Bulk Ingredient NDC: 50711-0008

Nonproprietary Name

dexmedetomidine hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT

50711-0008

Substance

DEXMEDETOMIDINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
30 Jun
Bulk Ingredient NDC: 50711-0009

Nonproprietary Name

Selenious Acid

Dosage Form

INJECTION

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0009

Substance

SELENIOUS ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-06-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
01 Sep
Bulk Ingredient NDC: 50711-0010

Nonproprietary Name

Chromic Chloride

Dosage Form

INJECTION

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT

50711-0010

Substance

CHROMIC CHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
23 Nov
Bulk Ingredient NDC: 50711-0011

Nonproprietary Name

Isoproterenol Hydrochloride

Dosage Form

INJECTION

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0011

Substance

ISOPROTERENOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-11-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
09 Oct
Bulk Ingredient NDC: 50711-0012

Nonproprietary Name

Cupric Sulfate Pentahydrate

Dosage Form

CRYSTAL

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0012

Substance

CUPRIC SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-10-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
18 Dec
Bulk Ingredient NDC: 50711-0014

Nonproprietary Name

4-Methylpyrazole

Dosage Form

INJECTION

Strength

1 g/g

Labeler

Strem Chemicals, Inc.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

50711-0014

Substance

FOMEPIZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-18

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).

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NDC Record Details Preview

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

NDC

50711-0013

Nonproprietary Name

Manganese Sulfate

Labeler

Strem Chemicals, Inc

Dosage Form

INJECTION

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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