Veranova
NDC Database

Veranova

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 4
  • Latest Marketing Date 2017-12-14
  • Data Source FDA
  • First Marketing Date 2017-12-11
Company Overview

Company

Veranova

Country

U.S.A

Website

Visit Website

Email

info@veranova.com

Social Profiles

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Company Snapshot

Veranova

435 Devon Park Drive, Suite 400, Wayne, PA. 19807

U.S.A

veranova.com/ info@veranova.com View on Map
NDC Records ( 4 records )
2017
14 Dec
Bulk Ingredient NDC: 12707-031

Nonproprietary Name

Apomorphine Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

MACFARLAN SMITH LIMITED

Marketing Category

BULK INGREDIENT

12707-031

Substance

APOMORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2017
14 Dec
Bulk Ingredient NDC: 12707-035

Nonproprietary Name

Buprenorphine Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Macfarlan Smith Limited

Marketing Category

BULK INGREDIENT

12707-035

Substance

BUPRENORPHINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2017-12-14

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2017
11 Dec
Bulk Ingredient NDC: 12707-036

Nonproprietary Name

Buprenorphine

Dosage Form

POWDER

Strength

100 g/100g

Labeler

Macfarlan Smith Limited

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

12707-036

Substance

BUPRENORPHINE

Product Type

BULK INGREDIENT

DEA Schedule

CIII

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2017
11 Dec
Bulk Ingredient NDC: 12707-037

Nonproprietary Name

Naloxone Hydrochloride Dihydrate

Dosage Form

POWDER

Strength

100 g/100g

Labeler

Macfarlan Smith Limited

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

12707-037

Substance

NALOXONE HYDROCHLORIDE DIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
4 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

12707-031

Nonproprietary Name

Apomorphine Hydrochloride

Labeler

MACFARLAN SMITH 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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