Lee Pharma
NDC Database

Lee 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 10
  • Latest Marketing Date 2026-04-01
  • Data Source FDA
  • First Marketing Date 2021-12-13
Company Overview

Company

Lee Pharma

Country

India

Website

Visit Website

Email

info@leepharma.com

Social Profiles

Company Snapshot

Lee Pharma

SY. No. : 257 & 258/1, Door No : 11-6/56-C, Opp : IDPL Factory, Moosapet, Balanagar ( Post ), Hyderabad – 500 037,

India

www.leepharma.com/ info@leepharma.com View on Map
NDC Records ( 10 records )
2021
13 Dec
Bulk Ingredient NDC: 75945-050

Nonproprietary Name

Rivaroxaban

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-050

Substance

RIVAROXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-13

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2021
14 Dec
Bulk Ingredient NDC: 75945-060

Nonproprietary Name

Apixaban

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-060

Substance

APIXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2022
09 Feb
Bulk Ingredient NDC: 75945-070

Nonproprietary Name

METAXALONE

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-070

Substance

METAXALONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
09 Feb
Bulk Ingredient NDC: 75945-070

Nonproprietary Name

Metaxalone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-070

Substance

METAXALONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
28 Jan
Bulk Ingredient NDC: 75945-700

Nonproprietary Name

Brivaracetam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-700

Substance

BRIVARACETAM

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2024-01-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
27 Jul
Bulk Ingredient NDC: 75945-800

Nonproprietary Name

Tofacitinib Citrate API

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-800

Substance

TOFACITINIB CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-07-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
19 Oct
Bulk Ingredient NDC: 75945-900

Nonproprietary Name

Finerenone API

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-900

Substance

FINERENONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-10-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
01 Dec
Bulk Ingredient NDC: 75945-902

Nonproprietary Name

Ticagrelor

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-902

Substance

TICAGRELOR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
01 Apr
Bulk Ingredient NDC: 75945-906

Nonproprietary Name

Lacosamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-906

Substance

LACOSAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2026-04-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Apr
Bulk Ingredient NDC: 75945-907

Nonproprietary Name

Amlodipine Besylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Lee Pharma Limited

Marketing Category

BULK INGREDIENT

75945-907

Substance

AMLODIPINE BESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-04-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
10 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

75945-050

Nonproprietary Name

Rivaroxaban

Labeler

Lee Pharma 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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