Aarti Pharmalabs
NDC Database

Aarti Pharmalabs

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 34
  • Latest Marketing Date 2025-03-03
  • Data Source FDA
  • First Marketing Date 1983-01-01
Company Overview

Company

Aarti Pharmalabs

Country

India

Social Profiles

LinkedIn
Company Snapshot

Aarti Pharmalabs

Embassy Park 247, Tower C, 401, 4th Floor, LBS Marg, Vikhroli (W), Mumbai

India

www.aartipharmalabs.com/ api@aartipharmalabs.com View on Map
NDC Records ( 34 records )
2001
01 Jan
Bulk Ingredient NDC: 15308-0100

Nonproprietary Name

Budesonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0100

Substance

BUDESONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
01 Jan
Bulk Ingredient NDC: 15308-0200

Nonproprietary Name

Fluticasone Propionate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0200

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
01 Jan
Bulk Ingredient NDC: 15308-0220

Nonproprietary Name

Mometasone Furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0220

Substance

MOMETASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
30 Aug
Bulk Ingredient NDC: 15308-0300

Nonproprietary Name

Ramipril

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0300

Substance

RAMIPRIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-08-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Jan
Bulk Ingredient NDC: 15308-0310

Nonproprietary Name

Levalbuterol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0310

Substance

LEVALBUTEROL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 Jan
Bulk Ingredient NDC: 15308-0320

Nonproprietary Name

Quetiapine Fumarate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0320

Substance

QUETIAPINE FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
01 Aug
Bulk Ingredient NDC: 15308-0360

Nonproprietary Name

Bicalutamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0360

Substance

BICALUTAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1990
01 Jan
Bulk Ingredient NDC: 15308-0411

Nonproprietary Name

Ifosfamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0411

Substance

IFOSFAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1990-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
24 Mar
Bulk Ingredient NDC: 15308-0412

Nonproprietary Name

BUPROPION HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0412

Substance

BUPROPION HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-03-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1992
01 Jan
Bulk Ingredient NDC: 15308-0500

Nonproprietary Name

Quinapril Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0500

Substance

QUINAPRIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1983
01 Jan
Bulk Ingredient NDC: 15308-0712

Nonproprietary Name

Mercaptopurine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0712

Substance

MERCAPTOPURINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1983-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1983
01 Jan
Bulk Ingredient NDC: 15308-0713

Nonproprietary Name

Desonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0713

Substance

DESONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1983-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1999
01 Jan
Bulk Ingredient NDC: 15308-0714

Nonproprietary Name

Capecitabine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0714

Substance

CAPECITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1999-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
01 Jan
Bulk Ingredient NDC: 15308-0715

Nonproprietary Name

Mesna

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0715

Substance

MESNA

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1997
01 Jan
Bulk Ingredient NDC: 15308-0716

Nonproprietary Name

Adapalene

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0716

Substance

ADAPALENE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1997-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
01 Jan
Bulk Ingredient NDC: 15308-0718

Nonproprietary Name

Ranolazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0718

Substance

RANOLAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
30 Jun
Bulk Ingredient NDC: 15308-0722

Nonproprietary Name

Loteprednol Etabonate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0722

Substance

LOTEPREDNOL ETABONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-06-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
03 Feb
Bulk Ingredient NDC: 15308-0732

Nonproprietary Name

AZATHIOPRINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0732

Substance

AZATHIOPRINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-02-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
08 Apr
Bulk Ingredient NDC: 15308-0811

Nonproprietary Name

Diflunisal

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0811

Substance

DIFLUNISAL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-04-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1992
01 Jan
Bulk Ingredient NDC: 15308-0900

Nonproprietary Name

Benazepril Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0900

Substance

BENAZEPRIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
27 Sep
Bulk Ingredient NDC: 15308-0921

Nonproprietary Name

Cyclophosphamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-0921

Substance

CYCLOPHOSPHAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-09-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1994
01 Jan
Bulk Ingredient NDC: 15308-1000

Nonproprietary Name

Perindopril Erbumine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1000

Substance

PERINDOPRIL ERBUMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1994-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
01 Jan
Bulk Ingredient NDC: 15308-1001

Nonproprietary Name

Ipratropium Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1001

Substance

IPRATROPIUM BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
21 Jan
Bulk Ingredient NDC: 15308-1021

Nonproprietary Name

Salmeterol Xinafoate

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1021

Substance

SALMETEROL XINAFOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-01-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
28 Apr
Bulk Ingredient NDC: 15308-1121

Nonproprietary Name

Enzalutamide

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1121

Substance

ENZALUTAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jul
Bulk Ingredient NDC: 15308-1221

Nonproprietary Name

Apixaban

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1221

Substance

APIXABAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
14 Dec
Bulk Ingredient NDC: 15308-1506

Nonproprietary Name

Venlafaxine Hydrochloride Polymorph B

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-1506

Substance

VENLAFAXINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
14 Jul
Bulk Ingredient NDC: 15308-2021

Nonproprietary Name

Fluticasone Furoate

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2021

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-07-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
31 Jan
Bulk Ingredient NDC: 15308-2401

Nonproprietary Name

Palbociclib

Dosage Form

POWDER

Strength

150 kg/150kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2401

Substance

PALBOCICLIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
31 Jan
Bulk Ingredient NDC: 15308-2402

Nonproprietary Name

Ibrutinib

Dosage Form

POWDER

Strength

200 kg/200kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2402

Substance

IBRUTINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
03 Mar
Bulk Ingredient NDC: 15308-2601

Nonproprietary Name

Enalapril Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2601

Substance

ENALAPRIL MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-03

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1998
01 Jan
Bulk Ingredient NDC: 15308-2610

Nonproprietary Name

Venlafaxine Hydrochloride Polymorph C

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2610

Substance

VENLAFAXINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
01 Jan
Bulk Ingredient NDC: 15308-2710

Nonproprietary Name

Mometasone Furoate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2710

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
16 Apr
Bulk Ingredient NDC: 15308-2908

Nonproprietary Name

Deferiprone

Dosage Form

POWDER

Strength

360 kg/360kg

Labeler

Aarti Pharmalabs Limited

Marketing Category

BULK INGREDIENT

15308-2908

Substance

DEFERIPRONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
34 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

15308-0100

Nonproprietary Name

Budesonide

Labeler

Aarti Pharmalabs 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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