Wanbury Limited
NDC Database

Wanbury 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 20
  • Latest Marketing Date 2021-12-28
  • Data Source FDA
  • First Marketing Date 2013-01-15
Company Overview

Company

Wanbury Limited

Country

India

Social Profiles

Company Snapshot

Wanbury Limited

Wanbury Limited BSEL Techpark,'B' Wing, 10th Floor,Sector 30-A,Opp. Vashi Railway Station, Vashi, Navi Mumbai - 400705

India

www.wanbury.com/ info@wanbury.com View on Map
NDC Records ( 20 records )
2013
15 Jan
Bulk Ingredient NDC: 62350-0015

Nonproprietary Name

MEFENAMIC ACID

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0015

Substance

MEFENAMIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
15 Jan
Bulk Ingredient NDC: 62350-0043

Nonproprietary Name

SERTRALINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0043

Substance

SERTRALINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
14 Dec
Bulk Ingredient NDC: 62350-0044

Nonproprietary Name

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0044

Substance

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
11 Jun
Bulk Ingredient NDC: 62350-0046

Nonproprietary Name

Tramadol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0046

Substance

TRAMADOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2021-06-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
15 Jan
Bulk Ingredient NDC: 62350-0047

Nonproprietary Name

DIPHENHYDRAMINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0047

Substance

DIPHENHYDRAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
28 Dec
Bulk Ingredient NDC: 62350-0047

Nonproprietary Name

Diphenhydramine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0047

Substance

DIPHENHYDRAMINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-12-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
01 Apr
Bulk Ingredient NDC: 62350-0048

Nonproprietary Name

DIPHENHYDRAMINE CITRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0048

Substance

DIPHENHYDRAMINE CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
15 Jan
Bulk Ingredient NDC: 62350-0049

Nonproprietary Name

METHOXSALEN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0049

Substance

METHOXSALEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
15 Jan
Bulk Ingredient NDC: 62350-0058

Nonproprietary Name

METFORMIN HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0058

Substance

METFORMIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-01-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
14 Dec
Bulk Ingredient NDC: 62350-0059

Nonproprietary Name

LEVETIRACETAM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0059

Substance

LEVETIRACETAM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
24 Jun
Bulk Ingredient NDC: 62350-0072

Nonproprietary Name

PREGABALIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0072

Substance

PREGABALIN

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2015-06-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
03 Feb
Bulk Ingredient NDC: 62350-0074

Nonproprietary Name

PAROXETINE MESYLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0074

Substance

PAROXETINE MESYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
03 Feb
Bulk Ingredient NDC: 62350-0075

Nonproprietary Name

SALSALATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0075

Substance

SALSALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
30 Jan
Bulk Ingredient NDC: 62350-0076

Nonproprietary Name

MESALAMINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0076

Substance

MESALAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-01-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
30 Jan
Bulk Ingredient NDC: 62350-0077

Nonproprietary Name

IMIQUIMOD

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0077

Substance

IMIQUIMOD

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-01-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
19 May
Bulk Ingredient NDC: 62350-0078

Nonproprietary Name

DOCUSATE SODIUM/SODIUM BENZOATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0078

Substance

DOCUSATE SODIUM/SODIUM BENZOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-05-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
10 Dec
Bulk Ingredient NDC: 62350-0080

Nonproprietary Name

HYDRALAZINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0080

Substance

HYDRALAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-12-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
29 Aug
Bulk Ingredient NDC: 62350-0081

Nonproprietary Name

DEXTROMETHORPHAN HYDROBROMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

62350-0081

Substance

DEXTROMETHORPHAN HYDROBROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-08-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 63155-1029

Nonproprietary Name

METFORMIN HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

63155-1029

Substance

METFORMIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
12 Jan
Bulk Ingredient NDC: 63155-1034

Nonproprietary Name

METFORMIN HYDROCHLORIDE DC

Dosage Form

GRANULE

Strength

1 kg/kg

Labeler

Wanbury Limited

Marketing Category

BULK INGREDIENT

63155-1034

Substance

METFORMIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
20 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

62350-0015

Nonproprietary Name

MEFENAMIC ACID

Labeler

Wanbury 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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