5N Plus Lubeck GmbH
NDC Database

5N Plus Lubeck GmbH

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 2022-01-01
  • Data Source FDA
  • First Marketing Date 1989-01-02
Company Overview

Company

5N Plus Lubeck GmbH

Country

Canada

Website

Visit Website

Email

info@5nplus.com

Social Profiles

Company Snapshot

5N Plus Lubeck GmbH

4385 Garand Street, Montreal, Quebec H4R 2B4

Canada

www.5nplus.com/ info@5nplus.com View on Map
NDC Records ( 7 records )
1992
01 Jan
Bulk Ingredient NDC: 47167-2221

Nonproprietary Name

Bismuth Citrate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-2221

Substance

BISMUTH CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1994
05 Jan
Bulk Ingredient NDC: 47167-3333

Nonproprietary Name

Bismuth subgallate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-3333

Substance

BISMUTH SUBGALLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1994-01-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1992
10 Jan
Bulk Ingredient NDC: 47167-4444

Nonproprietary Name

Bismuth subsalicylate

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-4444

Substance

BISMUTH SUBSALICYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1992-01-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2002
04 Jan
Bulk Ingredient NDC: 47167-5555

Nonproprietary Name

Bismuth Subsalicylate SG

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-5555

Substance

BISMUTH SUBSALICYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-01-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1989
02 Jan
Bulk Ingredient NDC: 47167-6666

Nonproprietary Name

Bismuth Subcarbonate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-6666

Substance

BISMUTH SUBCARBONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1989-01-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Jan
Bulk Ingredient NDC: 47167-7777

Nonproprietary Name

Bismuth Subcitrate Potassium

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-7777

Substance

BISMUTH SUBCITRATE POTASSIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Nov
Bulk Ingredient NDC: 47167-8888

Nonproprietary Name

Bismuth Subsalicylate SG Fine

Dosage Form

POWDER

Strength

500 kg/500kg

Labeler

5N Plus Lubeck GmbH

Marketing Category

BULK INGREDIENT

47167-8888

Substance

BISMUTH SUBSALICYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-11-01

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).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

47167-2221

Nonproprietary Name

Bismuth Citrate

Labeler

5N Plus Lubeck GmbH

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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