Embio Limited
NDC Database

Embio 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 5
  • Latest Marketing Date 2021-04-28
  • Data Source FDA
  • First Marketing Date 1998-12-29
Company Overview

Company

Embio Limited

Country

India

Website

Visit Website

Email

embio@embio.co.in

Social Profiles

Company Snapshot

Embio Limited

Embio Limited, 501, Sentinel, Hiranandani Gardens,Powai, Mumbai - 400 076 India

India

www.embio.co.in/ embio@embio.co.in View on Map
NDC Records ( 5 records )
1999
20 Jul
Bulk Ingredient NDC: 60646-101

Nonproprietary Name

Ephedrine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Embio Limited

Marketing Category

BULK INGREDIENT

60646-101

Substance

EPHEDRINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1999-07-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
29 Dec
Bulk Ingredient NDC: 60646-102

Nonproprietary Name

Pseudoephedrine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Embio Limited

Marketing Category

BULK INGREDIENT

60646-102

Substance

PSEUDOEPHEDRINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
31 Jan
Bulk Ingredient NDC: 60646-103

Nonproprietary Name

Pseudoephedrine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Embio Limited

Marketing Category

BULK INGREDIENT

60646-103

Substance

PSEUDOEPHEDRINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
11 Apr
Bulk Ingredient NDC: 60646-104

Nonproprietary Name

Ephedrine Sulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Embio Limited

Marketing Category

BULK INGREDIENT

60646-104

Substance

EPHEDRINE SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-04-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
28 Apr
Bulk Ingredient NDC: 60646-106

Nonproprietary Name

Selegiline Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Embio Limited

Marketing Category

BULK INGREDIENT

60646-106

Substance

SELEGILINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

Related Databases
  • FDA Inspections
    4 View
  • EDQM CEP
    2 View
  • KDMF
    0 View
  • Japan DMF
    3 View
  • Eudra GMP
    0 View
  • NDC Database
    5 View
  • FDA Approved Drugs Database
    0 View
  • Drug Prices in Switzerland
    0 View
NDC Type Breakdown
5 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

60646-101

Nonproprietary Name

Ephedrine Hydrochloride

Labeler

Embio 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.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit