Macleods Pharmaceuticals Limited
NDC Database

Macleods Pharmaceuticals Limited

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 2025-09-03
  • Data Source FDA
  • First Marketing Date 2015-11-17
Company Overview

Company

Macleods Pharmaceuticals Limited

Country

India

Website

Visit Website

Email

exports@macleodspharma.com

Social Profiles

Company Snapshot

Macleods Pharmaceuticals Limited

Atlanta Arcade, Marol Church Road, Andheri (East), Mumbai - 400059

India

www.macleodspharma.com/ exports@macleodspharma.com View on Map
NDC Records ( 13 records )
2015
17 Nov
Bulk Ingredient NDC: 33342-500

Nonproprietary Name

emtricitabine

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-500

Substance

EMTRICITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-11-17

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2015
17 Nov
Bulk Ingredient NDC: 33342-501

Nonproprietary Name

tenofovir disoproxil fumarate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-501

Substance

TENOFOVIR DISOPROXIL FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-11-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
16 Jan
Bulk Ingredient NDC: 33342-502

Nonproprietary Name

indomethacin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-502

Substance

INDOMETHACIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
23 Feb
Bulk Ingredient NDC: 33342-503

Nonproprietary Name

Levofloxacin hemihydrate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-503

Substance

LEVOFLOXACIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
24 Feb
Bulk Ingredient NDC: 33342-504

Nonproprietary Name

Vardenafil Hydrochloride Trihydrate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-504

Substance

VARDENAFIL HYDROCHLORIDE TRIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
02 Mar
Bulk Ingredient NDC: 33342-510

Nonproprietary Name

tenofovir alafenamide fumarate

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-510

Substance

TENOFOVIR ALAFENAMIDE FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
24 Jul
Bulk Ingredient NDC: 33342-600

Nonproprietary Name

Cycloserine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-600

Substance

CYCLOSERINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
02 Nov
Bulk Ingredient NDC: 33342-601

Nonproprietary Name

Lansoprazole

Dosage Form

POWDER

Strength

100 g/100g

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-601

Substance

LANSOPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-11-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
26 Feb
Bulk Ingredient NDC: 33342-602

Nonproprietary Name

Atomoxetine Hydrochloride

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-602

Substance

ATOMOXETINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-02-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
03 Sep
Bulk Ingredient NDC: 33342-605

Nonproprietary Name

Sacubitril-Valsartan

Dosage Form

POWDER

Strength

4 kg/4kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-605

Substance

SACUBITRIL VALSARTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-09-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
18 May
Bulk Ingredient NDC: 33342-606

Nonproprietary Name

linagliptin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-606

Substance

LINAGLIPTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-05-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2017
21 Sep
Bulk Ingredient NDC: 33342-607

Nonproprietary Name

oseltamivir phosphate

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-607

Substance

OSELTAMIVIR PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-09-21

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
24 Sep
Bulk Ingredient NDC: 33342-608

Nonproprietary Name

empagliflozin

Dosage Form

POWDER

Strength

15 kg/15kg

Labeler

Macleods Pharmaceuticals Limited

Marketing Category

BULK INGREDIENT

33342-608

Substance

EMPAGLIFLOZIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-09-24

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

33342-500

Nonproprietary Name

emtricitabine

Labeler

Macleods Pharmaceuticals 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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