Aurore Life Sciences
NDC Database

Aurore Life Sciences

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 32
  • Latest Marketing Date 2026-05-01
  • Data Source FDA
  • First Marketing Date 2019-02-05
Company Overview

Company

Aurore Life Sciences

Country

India

Social Profiles

LinkedIn
Company Snapshot

Aurore Life Sciences

Jubilee Heights, 2nd Floor, Beside Shilparamam, Hitech City, Hyderabad – 500 081

India

www.aurorels.com/ sales@aurorels.com View on Map
NDC Records ( 32 records )
2019
09 Feb
Bulk Ingredient NDC: 72761-001

Nonproprietary Name

ARMODANFINIL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-001

Substance

ARMODAFINIL

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2019-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Feb
Bulk Ingredient NDC: 72761-002

Nonproprietary Name

CANDESARTAN CILEXETIL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-002

Substance

CANDESARTAN CILEXETIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Feb
Bulk Ingredient NDC: 72761-004

Nonproprietary Name

CARVEDILOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-004

Substance

CARVEDILOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 Mar
Bulk Ingredient NDC: 72761-006

Nonproprietary Name

Citalopram Hydrobromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-006

Substance

CITALOPRAM HYDROBROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 Mar
Bulk Ingredient NDC: 72761-007

Nonproprietary Name

Emtricitabine (Process -II)

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-007

Substance

EMTRICITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 Mar
Bulk Ingredient NDC: 72761-008

Nonproprietary Name

Emtricitabine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-008

Substance

EMTRICITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 Mar
Bulk Ingredient NDC: 72761-009

Nonproprietary Name

Escitalopram oxalate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-009

Substance

ESCITALOPRAM OXALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Feb
Bulk Ingredient NDC: 72761-010

Nonproprietary Name

Esomeprazole Magnesium Trihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-010

Substance

ESOMEPRAZOLE MAGNESIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
09 Feb
Bulk Ingredient NDC: 72761-011

Nonproprietary Name

Esomeprazole Magnesium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-011

Substance

ESOMEPRAZOLE MAGNESIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
05 Feb
Bulk Ingredient NDC: 72761-012

Nonproprietary Name

Esomprazole Magnesium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-012

Substance

ESOMEPRAZOLE MAGNESIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-02-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
16 Mar
Bulk Ingredient NDC: 72761-013

Nonproprietary Name

Eszopiclone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-013

Substance

ESZOPICLONE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2019-03-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
22 Mar
Bulk Ingredient NDC: 72761-015

Nonproprietary Name

Mirtazapine Anhydrous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-015

Substance

MIRTAZAPINE HEMIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
22 Mar
Bulk Ingredient NDC: 72761-017

Nonproprietary Name

Tadalafil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-017

Substance

TADALAFIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
22 Mar
Bulk Ingredient NDC: 72761-018

Nonproprietary Name

Venlafaxine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-018

Substance

VENLAFAXINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
22 Mar
Bulk Ingredient NDC: 72761-019

Nonproprietary Name

Itraconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-019

Substance

ITRACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
22 Mar
Bulk Ingredient NDC: 72761-021

Nonproprietary Name

Telmisartan

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-021

Substance

TELMISARTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
05 Aug
Bulk Ingredient NDC: 72761-023

Nonproprietary Name

MODAFINIL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-023

Substance

MODAFINIL

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2019-08-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
18 Jul
Bulk Ingredient NDC: 72761-025

Nonproprietary Name

VALACYCLOVIR HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-025

Substance

VALACYCLOVIR HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-07-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
15 Dec
Bulk Ingredient NDC: 72761-026

Nonproprietary Name

Levothyroxine Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-026

Substance

LEVOTHYROXINE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
10 Dec
Bulk Ingredient NDC: 72761-027

Nonproprietary Name

SALSALATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-027

Substance

SALSALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-12-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
25 Jul
Bulk Ingredient NDC: 72761-028

Nonproprietary Name

NAFAMOSTAT MESYLATE JP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-028

Substance

NAFAMOSTAT MESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-07-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
08 May
Bulk Ingredient NDC: 72761-029

Nonproprietary Name

VALGANCICLOVIR HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-029

Substance

VALGANCICLOVIR HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-05-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
07 Jul
Bulk Ingredient NDC: 72761-030

Nonproprietary Name

VERAPAMIL HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-030

Substance

VERAPAMIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
06 Dec
Bulk Ingredient NDC: 72761-031

Nonproprietary Name

REMDESIVIR

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-031

Substance

REMDESIVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
20 Sep
Bulk Ingredient NDC: 72761-032

Nonproprietary Name

TOLVAPTAN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-032

Substance

TOLVAPTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-09-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
28 Feb
Bulk Ingredient NDC: 72761-033

Nonproprietary Name

Oxcarbazepine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-033

Substance

OXCARBAZEPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
22 Jul
Bulk Ingredient NDC: 72761-034

Nonproprietary Name

AMLODIPINE BESYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

AURORE PHARMACEUTICALS PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

72761-034

Substance

AMLODIPINE BESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-07-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
10 Jan
Bulk Ingredient NDC: 72761-036

Nonproprietary Name

TOFACITINIB CITRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-036

Substance

TOFACITINIB CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
25 Nov
Bulk Ingredient NDC: 72761-038

Nonproprietary Name

RILPIVIRINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore pharmaceuticals private limited

Marketing Category

BULK INGREDIENT

72761-038

Substance

RILPIVIRINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Sep
Bulk Ingredient NDC: 72761-039

Nonproprietary Name

cromolyn sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-039

Substance

CROMOLYN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Dec
Bulk Ingredient NDC: 72761-040

Nonproprietary Name

Indomethacin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-040

Substance

INDOMETHACIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
01 May
Bulk Ingredient NDC: 72761-041

Nonproprietary Name

Clozapine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Aurore Pharmaceuticals Private Limited

Marketing Category

BULK INGREDIENT

72761-041

Substance

CLOZAPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-05-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
32 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

72761-001

Nonproprietary Name

ARMODANFINIL

Labeler

AURORE PHARMACEUTICALS PRIVATE 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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