Sun Pharmaceutical Industries Limited
NDC Database

Sun Pharmaceutical Industries 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 6
  • Latest Marketing Date 2026-06-05
  • Data Source FDA
  • First Marketing Date 2026-05-18
Company Overview

Company

Sun Pharmaceutical Industries Limited

Country

India

Website

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Company Snapshot

Sun Pharmaceutical Industries Limited

Sun House, CTS No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063

India

sunpharma.com/ View on Map
NDC Records ( 6 records )
2026
18 May
Bulk Ingredient NDC: 54907-0134

Nonproprietary Name

Prucalopride Succinate - 1.0

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0134

Substance

PRUCALOPRIDE SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-05-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
05 Jun
Bulk Ingredient NDC: 54907-0137

Nonproprietary Name

Erlotinib Hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0137

Substance

ERLOTINIB HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
05 Jun
Bulk Ingredient NDC: 54907-0138

Nonproprietary Name

Canagliflozin crystalline

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0138

Substance

CANAGLIFLOZIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
05 Jun
Bulk Ingredient NDC: 54907-0139

Nonproprietary Name

Sunitinib Malate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0139

Substance

SUNITINIB MALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
05 Jun
Bulk Ingredient NDC: 54907-0140

Nonproprietary Name

Lumacaftor

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0140

Substance

LUMACAFTOR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
05 Jun
Bulk Ingredient NDC: 54907-0141

Nonproprietary Name

Cariprazine Hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Sun Pharmaceutical Industries Limited

Marketing Category

BULK INGREDIENT

54907-0141

Substance

CARIPRAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
6 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).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

54907-0134

Nonproprietary Name

Prucalopride Succinate - 1.0

Labeler

Sun Pharmaceutical Industries Limited

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

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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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