3M Company
FDA Approved Drugs

3M Company

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued

Total Records 32
Latest Approval Date Jul 16, 1987
Data Source FDA
First Approval Date Jan 01, 1982

Company Overview

Company

3M Company

Country

U.S.A

Website

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Company Snapshot

3M Company

3M CenterBuilding 275-03-E-10St. Paul, MN 55144-1000

U.S.A

www.3m.com/ View on Map

FDA Approved Drug Records ( 32 records )

1982

01 Jan

Discontinued Application: 84868

Drug Name

CIRCANOL

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1982-01-01

84868 / 1 View Details

Active Ingredient

ERGOLOID MESYLATES

Application Number

84868

Product Number

Dosage Form

Strength

0.5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85809

Drug Name

CIRCANOL

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

85809 / 1 View Details

Active Ingredient

ERGOLOID MESYLATES

Application Number

85809

Product Number

Dosage Form

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10653

Drug Name

DISIPAL

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

10653 / 1 View Details

Active Ingredient

ORPHENADRINE HYDROCHLORIDE

Application Number

10653

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 13296

Drug Name

DUO-MEDIHALER

Product Number

Dosage Form

Strength

0.16MG/INH;0.24MG/INH

Approval Date

1982-01-01

13296 / 1 View Details

Active Ingredient

ISOPROTERENOL HYDROCHLORIDE; PHENYLEPHRINE BITARTRATE

Application Number

13296

Product Number

Dosage Form

Strength

0.16MG/INH;0.24MG/INH

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10375

Drug Name

ISOPROTERENOL HYDROCHLORIDE

Product Number

Dosage Form

Strength

0.12MG/INH

Approval Date

1982-01-01

10375 / 4 View Details

Active Ingredient

ISOPROTERENOL HYDROCHLORIDE

Application Number

10375

Product Number

Dosage Form

Strength

0.12MG/INH

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

1,000 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 1 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

1,000 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

5,000 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 2 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

5,000 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

10,000 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 3 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

10,000 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

20,000 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 4 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

20,000 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

40,000 UNITS/ML

Approval Date

1982-01-01

17027 / 5 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

40,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

17027 / 6 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

1,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

20,000 UNITS/ML

Approval Date

1982-01-01

17027 / 7 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

20,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

17027 / 8 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

5,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

17027 / 9 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

10,000 UNITS/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

7,500 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 10 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

7,500 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17027

Drug Name

LIPO-HEPIN

Product Number

Dosage Form

Strength

15,000 UNITS/0.5ML

Approval Date

1982-01-01

17027 / 11 View Details

Active Ingredient

HEPARIN SODIUM

Application Number

17027

Product Number

Dosage Form

Strength

15,000 UNITS/0.5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 12102

Drug Name

MEDIHALER ERGOTAMINE

Product Number

Dosage Form

Strength

0.36MG/INH

Approval Date

1982-01-01

12102 / 1 View Details

Active Ingredient

ERGOTAMINE TARTRATE

Application Number

12102

Product Number

Dosage Form

Strength

0.36MG/INH

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10374

Drug Name

MEDIHALER-EPI

Product Number

Dosage Form

Strength

0.3MG/INH

Approval Date

1982-01-01

10374 / 3 View Details

Active Ingredient

EPINEPHRINE BITARTRATE

Application Number

10374

Product Number

Dosage Form

Strength

0.3MG/INH

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 10375

Drug Name

MEDIHALER-ISO

Product Number

Dosage Form

Strength

0.08MG/INH

Approval Date

1982-01-01

10375 / 3 View Details

Active Ingredient

ISOPROTERENOL SULFATE

Application Number

10375

Product Number

Dosage Form

Strength

0.08MG/INH

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 8867

Drug Name

RAUWILOID

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

8867 / 1 View Details

Active Ingredient

ALSEROXYLON

Application Number

8867

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17413

Drug Name

SCRUBTEAM SURGICAL SPONGEBRUSH

Product Number

Dosage Form

Strength

330MG

Approval Date

1982-01-01

17413 / 1 View Details

Active Ingredient

HEXACHLOROPHENE

Application Number

17413

Product Number

Dosage Form

Strength

330MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 11673

Drug Name

TEPANIL

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

11673 / 1 View Details

Active Ingredient

DIETHYLPROPION HYDROCHLORIDE

Application Number

11673

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17956

Drug Name

TEPANIL TEN-TAB

Product Number

Dosage Form

Strength

75MG

Approval Date

1982-01-01

17956 / 1 View Details

Active Ingredient

DIETHYLPROPION HYDROCHLORIDE

Application Number

17956

Product Number

Dosage Form

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86107

Drug Name

THEOLAIR

Product Number

Dosage Form

Strength

80MG/15ML

Approval Date

1982-01-01

86107 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

86107

Product Number

Dosage Form

Strength

80MG/15ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

16 Jul

Discontinued Application: 86363

Drug Name

THEOLAIR-SR

Product Number

Dosage Form

Strength

250MG

Approval Date

1987-07-16

86363 / 2 View Details

Active Ingredient

THEOPHYLLINE

Application Number

86363

Product Number

Dosage Form

Strength

250MG

Approval Date

1987-07-16

Regulatory Status

Discontinued

1987

16 Jul

Discontinued Application: 88364

Drug Name

THEOLAIR-SR

Product Number

Dosage Form

Strength

300MG

Approval Date

1987-07-16

88364 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

88364

Product Number

Dosage Form

Strength

300MG

Approval Date

1987-07-16

Regulatory Status

Discontinued

1987

16 Jul

Discontinued Application: 88369

Drug Name

THEOLAIR-SR

Product Number

Dosage Form

Strength

200MG

Approval Date

1987-07-16

88369 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

88369

Product Number

Dosage Form

Strength

200MG

Approval Date

1987-07-16

Regulatory Status

Discontinued

1987

16 Jul

Discontinued Application: 89132

Drug Name

THEOLAIR-SR

Product Number

Dosage Form

Strength

500MG

Approval Date

1987-07-16

89132 / 1 View Details

Active Ingredient

THEOPHYLLINE

Application Number

89132

Product Number

Dosage Form

Strength

500MG

Approval Date

1987-07-16

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 12126

Drug Name

ULO

Product Number

Dosage Form

Strength

25MG/5ML

Approval Date

1982-01-01

12126 / 1 View Details

Active Ingredient

CHLOPHEDIANOL HYDROCHLORIDE

Application Number

12126

Product Number

Dosage Form

Strength

25MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7336

Drug Name

VERILOID

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

7336 / 2 View Details

Active Ingredient

ALKAVERVIR

Application Number

7336

Product Number

Dosage Form

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 7336

Drug Name

VERILOID

Product Number

Dosage Form

Strength

3MG

Approval Date

1982-01-01

7336 / 3 View Details

Active Ingredient

ALKAVERVIR

Application Number

7336

Product Number

Dosage Form

Strength

3MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 17518

Drug Name

YTTERBIUM YB 169 DTPA

Product Number

Dosage Form

Strength

2mCi/ML

Approval Date

1982-01-01

17518 / 1 View Details

Active Ingredient

PENTETATE CALCIUM TRISODIUM YB-169

Application Number

17518

Product Number

Dosage Form

Strength

2mCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

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FDA Approved Drugs Database
32 View

Drug Status Breakdown

32 total

Discontinued

Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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Drug Name

CIRCANOL

Application Number

84868

Product Number

Active Ingredient

ERGOLOID MESYLATES

Dosage Form

Strength

0.5MG

FDA Approved Drug Data

Approved drug product information

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