Steriscience
FDA Approved Drugs

Steriscience

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.

RX Discontinued
  • Total Records 21
  • Latest Approval Date Jul 28, 2026
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
21
View
Discontinued
9
View
RX
12
View
Company Overview

Company

Steriscience

Country

India

Website

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Company Snapshot

Steriscience

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

India

steri-science.com/ View on Map
FDA Approved Drug Records ( 21 records )
2025
06 Nov
RX Application: 217972

Drug Name

DOXYCYCLINE HYCLATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

2025-11-06

217972 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

217972

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

Approval Date

2025-11-06

Regulatory Status

RX

2023
22 Aug
RX Application: 216686

Drug Name

FOCINVEZ

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/50ML (EQ 3MG BASE/ML)

Approval Date

2023-08-22

216686 / 1

Active Ingredient

FOSAPREPITANT DIMEGLUMINE

Application Number

216686

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/50ML (EQ 3MG BASE/ML)

Approval Date

2023-08-22

Regulatory Status

RX

2024
22 Nov
RX Application: 216955

Drug Name

METHYLENE BLUE

Product Number

1

Dosage Form

-

Strength

50MG/10ML (5MG/ML)

Approval Date

2024-11-22

216955 / 1

Active Ingredient

METHYLENE BLUE

Application Number

216955

Product Number

1

Dosage Form

-

Strength

50MG/10ML (5MG/ML)

Approval Date

2024-11-22

Regulatory Status

RX

2024
22 Jul
RX Application: 217092

Drug Name

ROCURONIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2024-07-22

217092 / 1

Active Ingredient

ROCURONIUM BROMIDE

Application Number

217092

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2024-07-22

Regulatory Status

RX

2023
28 Jun
RX Application: 217594

Drug Name

SODIUM BICARBONATE

Product Number

1

Dosage Form

-

Strength

50MEQ/50ML (1MEQ/ML)

Approval Date

2023-06-28

217594 / 1

Active Ingredient

SODIUM BICARBONATE

Application Number

217594

Product Number

1

Dosage Form

-

Strength

50MEQ/50ML (1MEQ/ML)

Approval Date

2023-06-28

Regulatory Status

RX

2024
09 Jul
RX Application: 217873

Drug Name

SUCCINYLCHOLINE CHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

2024-07-09

217873 / 1

Active Ingredient

SUCCINYLCHOLINE CHLORIDE

Application Number

217873

Product Number

1

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

2024-07-09

Regulatory Status

RX

2026
28 Jul
RX Application: 218814

Drug Name

SUGAMMADEX SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/2ML (EQ 100MG BASE/ML)

Approval Date

2026-07-28

218814 / 1

Active Ingredient

SUGAMMADEX SODIUM

Application Number

218814

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/2ML (EQ 100MG BASE/ML)

Approval Date

2026-07-28

Regulatory Status

RX

2026
28 Jul
RX Application: 218814

Drug Name

SUGAMMADEX SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/5ML (EQ 100MG BASE/ML)

Approval Date

2026-07-28

218814 / 2

Active Ingredient

SUGAMMADEX SODIUM

Application Number

218814

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/5ML (EQ 100MG BASE/ML)

Approval Date

2026-07-28

Regulatory Status

RX

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

2025
02 Oct
RX Application: 215324

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

2025-10-02

215324 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

215324

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

2025-10-02

Regulatory Status

RX

2025
02 Oct
RX Application: 215324

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1.25GM BASE/VIAL

Approval Date

2025-10-02

215324 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

215324

Product Number

2

Dosage Form

-

Strength

EQ 1.25GM BASE/VIAL

Approval Date

2025-10-02

Regulatory Status

RX

2025
02 Oct
RX Application: 215324

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

2025-10-02

215324 / 3

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

215324

Product Number

3

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

2025-10-02

Regulatory Status

RX

2025
03 Sep
RX Application: 217595

Drug Name

ZIPRASIDONE MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/VIAL

Approval Date

2025-09-03

217595 / 1

Active Ingredient

ZIPRASIDONE MESYLATE

Application Number

217595

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/VIAL

Approval Date

2025-09-03

Regulatory Status

RX

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Drug Status Breakdown
21 total
  • RX
  • Discontinued
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

DOXYCYCLINE HYCLATE

Application Number

217972

Product Number

1

Active Ingredient

DOXYCYCLINE HYCLATE

Dosage Form

-

Strength

EQ 100MG BASE/VIAL

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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