Steriscience RX
FDA Approved Drugs

Steriscience RX

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
  • Total Records 12
  • Latest Approval Date Jul 28, 2026
  • Data Source FDA
  • First Approval Date Jun 28, 2023
All
21
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Discontinued
9
View
RX
12
View
Company Overview

Company

Steriscience RX

Country

India

Email

Social Profiles

Company Snapshot

Steriscience RX

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

India

steri-science.com/ View on Map
FDA Approved Drug Records ( 12 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

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
12 total
  • RX
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

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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