Rusan Pharma
NDC Database

Rusan Pharma

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 5
  • Latest Marketing Date 2026-04-08
  • Data Source FDA
  • First Marketing Date 2015-12-16
Company Overview

Company

Rusan Pharma

Country

India

Website

Visit Website

Email

enquiry@rusanpharma.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Rusan Pharma

58-D, Government Industrial Estate, Charkop, Kandivali (West), Mumbai – 400 067 Maharashtra

India

www.rusanpharma.com/ enquiry@rusanpharma.com View on Map
NDC Records ( 5 records )
2015
16 Dec
Bulk Ingredient NDC: 70312-0887

Nonproprietary Name

Naltrexone Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

RUSAN PHARMA LTD

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

70312-0887

Substance

NALTREXONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-12-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
19 Jan
Bulk Ingredient NDC: 70312-0888

Nonproprietary Name

Naltrexone base

Dosage Form

POWDER

Strength

1 g/g

Labeler

Rusan Pharma Ltd

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

70312-0888

Substance

NALTREXONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-01-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
04 Jan
Bulk Ingredient NDC: 70312-0889

Nonproprietary Name

Eflornithine Hydrochloride monohydrate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Rusan Pharma Ltd

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

70312-0889

Substance

EFLORNITHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
09 Mar
Bulk Ingredient NDC: 70312-0890

Nonproprietary Name

Apomorphine Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Rusan Pharma Ltd

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

70312-0890

Substance

APOMORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-03-09

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
08 Apr
Bulk Ingredient NDC: 70312-0891

Nonproprietary Name

Nalbuphine Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Rusan Pharma Ltd

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

70312-0891

Substance

NALBUPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-04-08

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
5 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

70312-0887

Nonproprietary Name

Naltrexone Hydrochloride

Labeler

RUSAN PHARMA LTD

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

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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