Alchem International Private Ltd
NDC Database

Alchem International Private Ltd

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 2024-11-07
  • Data Source FDA
  • First Marketing Date 2011-02-02
Company Overview

Company

Alchem International Private Ltd

Country

India

Social Profiles

Company Snapshot

Alchem International Private Ltd

201, Empire Plaza, Mehrauli - Gurgaon Road, Sultanpur, New Delhi-110 030

India

www.alcheminternational.com/ geeta@alcheminternational.com View on Map
NDC Records ( 13 records )
2012
01 Jan
Bulk Ingredient NDC: 55742-003

Nonproprietary Name

Nicotine

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-003

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
31 May
Bulk Ingredient NDC: 55742-007

Nonproprietary Name

Sennosides

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-007

Substance

SENNOSIDES

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
22 Apr
Bulk Ingredient NDC: 55742-011

Nonproprietary Name

Scopolamine Hydrobromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-011

Substance

SCOPOLAMINE HYDROBROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-04-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
25 Jul
Bulk Ingredient NDC: 55742-013

Nonproprietary Name

Hyoscyamine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-013

Substance

HYOSCYAMINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-07-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
06 Jan
Bulk Ingredient NDC: 55742-014

Nonproprietary Name

Methscopolamine Bromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-014

Substance

METHSCOPOLAMINE BROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
02 Feb
Bulk Ingredient NDC: 55742-123

Nonproprietary Name

Digoxin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-123

Substance

DIGOXIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-02-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
15 Sep
Bulk Ingredient NDC: 55742-124

Nonproprietary Name

ATROPINE SULFATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-124

Substance

ATROPINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
31 Aug
Bulk Ingredient NDC: 55742-125

Nonproprietary Name

NICOTINE BITARTRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-125

Substance

NICOTINE BITARTRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-08-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
15 Sep
Bulk Ingredient NDC: 55742-126

Nonproprietary Name

SCOPOLAMINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-126

Substance

SCOPOLAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-09-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
23 Dec
Bulk Ingredient NDC: 55742-127

Nonproprietary Name

Colchicine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-127

Substance

COLCHICINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-12-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
23 Dec
Bulk Ingredient NDC: 55742-128

Nonproprietary Name

Nicotine Polacrilex

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-128

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-12-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
17 Jan
Bulk Ingredient NDC: 55742-129

Nonproprietary Name

NICOTINE SALICYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-129

Substance

NICOTINE SALICYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
07 Nov
Bulk Ingredient NDC: 55742-130

Nonproprietary Name

Enoxolone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Alchem International Private Ltd

Marketing Category

BULK INGREDIENT

55742-130

Substance

ENOXOLONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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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

55742-003

Nonproprietary Name

Nicotine

Labeler

Alchem International Private Ltd

Dosage Form

LIQUID

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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