Enaltec Labs Private Limited
NDC Database

Enaltec Labs Private 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 7
  • Latest Marketing Date 2017-12-29
  • Data Source FDA
  • First Marketing Date 2011-05-27
Company Overview

Company

Enaltec Labs Private Limited

Country

India

Social Profiles

Company Snapshot

Enaltec Labs Private Limited

1706, 17th Floor, Kesar Solitaire, Plot No. 5, Sector 19, Sanpada, Navi Mumbai – 400 705

India

enalteclabs.co.in/home.php info@enalteclabs.co.in View on Map
NDC Records ( 7 records )
2011
27 May
Bulk Ingredient NDC: 42413-0007

Nonproprietary Name

Bromfenac Sodium (Sesquihydrate)

Dosage Form

POWDER

Strength

1 g/g

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0007

Substance

BROMFENAC SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-05-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
28 Nov
Bulk Ingredient NDC: 42413-0014

Nonproprietary Name

Nepafenac (Non-Sterile)

Dosage Form

POWDER

Strength

1.375 kg/1.375kg

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0014

Substance

NEPAFENAC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
28 Nov
Bulk Ingredient NDC: 42413-0049

Nonproprietary Name

Tetrabenzine

Dosage Form

POWDER

Strength

5.46 kg/5.46kg

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0049

Substance

TETRABENAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
12 Mar
Bulk Ingredient NDC: 42413-0059

Nonproprietary Name

Ethacrynic acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0059

Substance

ETHACRYNIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
29 Dec
Bulk Ingredient NDC: 42413-0060

Nonproprietary Name

Dronedarone Hydrochloride

Dosage Form

POWDER

Strength

36.215 kg/36.215kg

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0060

Substance

DRONEDARONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-29

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
13 Mar
Bulk Ingredient NDC: 42413-0062

Nonproprietary Name

Ethacrynate Sodium

Dosage Form

POWDER

Strength

1 g/g

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0062

Substance

ETHACRYNATE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
28 Nov
Bulk Ingredient NDC: 42413-0092

Nonproprietary Name

Nepafenac (Sterile)

Dosage Form

POWDER

Strength

0.375 kg/.375kg

Labeler

Enaltec Labs Private Limited

Marketing Category

BULK INGREDIENT

42413-0092

Substance

NEPAFENAC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
7 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

42413-0007

Nonproprietary Name

Bromfenac Sodium (Sesquihydrate)

Labeler

Enaltec Labs 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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