Steriscience Discontinued
FDA Approved Drugs

Steriscience Discontinued

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 9
  • Latest Approval Date Nov 17, 1987
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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21
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Discontinued
9
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RX
12
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Company Overview

Company

Steriscience Discontinued

Country

India

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Company Snapshot

Steriscience Discontinued

Plot No 30, Galaxy, 1st Main Road,J.P. Nagar, Third Phase,,Karnataka

India

steri-science.com/ View on Map
FDA Approved Drug Records ( 9 records )
1982
01 Jan
Discontinued Application: 60180

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

60180 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

60180

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
21 Mar
Discontinued Application: 60180

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-03-21

60180 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

60180

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-03-21

Regulatory Status

Discontinued

1984
15 Mar
Discontinued Application: 62476

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-03-15

62476 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62476

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1984-03-15

Regulatory Status

Discontinued

1986
21 Mar
Discontinued Application: 62476

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-21

62476 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62476

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1986-03-21

Regulatory Status

Discontinued

1987
13 Mar
Discontinued Application: 62716

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1987-03-13

62716 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62716

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1987-03-13

Regulatory Status

Discontinued

1987
13 Mar
Discontinued Application: 62716

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-03-13

62716 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62716

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-03-13

Regulatory Status

Discontinued

1987
17 Nov
Discontinued Application: 62812

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

62812 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62812

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

Regulatory Status

Discontinued

1987
17 Nov
Discontinued Application: 62812

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

62812 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62812

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

Regulatory Status

Discontinued

1987
17 Nov
Discontinued Application: 62812

Drug Name

VANCOCIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

62812 / 3

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

62812

Product Number

3

Dosage Form

-

Strength

EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-11-17

Regulatory Status

Discontinued

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Drug Status Breakdown
9 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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Explore important FDA approved drug information available in the records above.

Drug Name

VANCOCIN HYDROCHLORIDE

Application Number

60180

Product Number

1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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