Hybio Pharmaceutical RX
FDA Approved Drugs

Hybio Pharmaceutical 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 2
  • Latest Approval Date Feb 11, 2026
  • Data Source FDA
  • First Approval Date Feb 11, 2026
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4
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Discontinued
2
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RX
2
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Company Overview

Company

Hybio Pharmaceutical RX

Country

China

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Company Snapshot

Hybio Pharmaceutical RX

No.37, Keji C.2nd Hybio Medicine Park Guangdong

China

www.hybio.com.cn/en-us View on Map
FDA Approved Drug Records ( 2 records )
2026
11 Feb
RX Application: 213382

Drug Name

GLATIRAMER ACETATE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2026-02-11

213382 / 1

Active Ingredient

GLATIRAMER ACETATE

Application Number

213382

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2026-02-11

Regulatory Status

RX

2026
11 Feb
RX Application: 214022

Drug Name

GLATIRAMER ACETATE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2026-02-11

214022 / 1

Active Ingredient

GLATIRAMER ACETATE

Application Number

214022

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2026-02-11

Regulatory Status

RX

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Drug Status Breakdown
2 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

GLATIRAMER ACETATE

Application Number

213382

Product Number

1

Active Ingredient

GLATIRAMER ACETATE

Dosage Form

-

Strength

20MG/ML

FDA Approved Drug Data

Approved drug product information

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