Lupin Ltd
NDC Database

Lupin Ltd

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 13
  • Latest Marketing Date 2026-04-04
  • Data Source FDA
  • First Marketing Date 1998-04-30
Company Overview

Company

Lupin Ltd

Country

India

Website

Visit Website

Email

info@lupin.com

Social Profiles

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Company Snapshot

Lupin Ltd

Kalina, Santacruz East, Mumbai 400 098

India

www.lupin.com/ info@lupin.com View on Map
NDC Records ( 13 records )
2010
01 Jun
Bulk Ingredient NDC: 57297-029

Nonproprietary Name

rifaximin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-029

Substance

RIFAXIMIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
20 Mar
Bulk Ingredient NDC: 57297-330

Nonproprietary Name

Ziprasidone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-330

Substance

ZIPRASIDONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-03-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
25 Feb
Bulk Ingredient NDC: 57297-400

Nonproprietary Name

Cefprozil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-400

Substance

CEFPROZIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
30 Apr
Bulk Ingredient NDC: 57297-444

Nonproprietary Name

Rifampin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-444

Substance

RIFAMPIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-04-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
18 Oct
Bulk Ingredient NDC: 57297-511

Nonproprietary Name

Lisinopril

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-511

Substance

LISINOPRIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-10-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
09 Jun
Bulk Ingredient NDC: 57297-700

Nonproprietary Name

Cefdinir Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-700

Substance

CEFDINIR MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
05 Dec
Bulk Ingredient NDC: 57297-977

Nonproprietary Name

Levothyroxine Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

57297-977

Substance

LEVOTHYROXINE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
07 Nov
Bulk Ingredient NDC: 71586-006

Nonproprietary Name

Fluticasone Furoate (Micronized)

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

71586-006

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
08 Dec
Bulk Ingredient NDC: 71586-007

Nonproprietary Name

Umeclidinium Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN LIMITED

Marketing Category

BULK INGREDIENT

71586-007

Substance

UMECLIDINIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-12-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Nov
Bulk Ingredient NDC: 83786-001

Nonproprietary Name

Ferric Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN MANUFACTURING SOLUTIONS LIMITED

Marketing Category

BULK INGREDIENT

83786-001

Substance

FERRIC CITRATE ANHYDROUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
13 Dec
Bulk Ingredient NDC: 83786-009

Nonproprietary Name

Glycerol Phenylbutyrate

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

LUPIN MANUFACTURING SOLUTIONS LIMITED

Marketing Category

BULK INGREDIENT

83786-009

Substance

GLYCEROL PHENYLBUTYRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-12-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
05 Mar
Bulk Ingredient NDC: 83786-010

Nonproprietary Name

Eslicarbazepine Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN MANUFACTURING SOLUTIONS LIMITED

Marketing Category

BULK INGREDIENT

83786-010

Substance

ESLICARBAZEPINE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
04 Apr
Bulk Ingredient NDC: 83786-011

Nonproprietary Name

Deutetrabenazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

LUPIN MANUFACTURING SOLUTIONS LIMITED

Marketing Category

BULK INGREDIENT

83786-011

Substance

DEUTETRABENAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-04-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
13 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

57297-029

Nonproprietary Name

rifaximin

Labeler

LUPIN LIMITED

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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