Sichuan Qingmu Pharmaceutical RX
FDA Approved Drugs

Sichuan Qingmu 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 4
  • Latest Approval Date Dec 23, 2025
  • Data Source FDA
  • First Approval Date Nov 15, 2023
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Unclassified
1
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RX
4
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Company Overview

Company

Sichuan Qingmu Pharmaceutical RX

Country

China

Website

Visit Website

Email

sales@eastonpharma.cn

Social Profiles

Company Snapshot

Sichuan Qingmu Pharmaceutical RX

Ankang Road, Shuangliu District, Chengdu City, Sichuan Province

China

www.qingmupharm.com sales@eastonpharma.cn View on Map
FDA Approved Drug Records ( 4 records )
2025
23 Dec
RX Application: 219550

Drug Name

METHYLENE BLUE

Product Number

1

Dosage Form

-

Strength

50MG/10ML (5MG/ML)

Approval Date

2025-12-23

219550 / 1

Active Ingredient

METHYLENE BLUE

Application Number

219550

Product Number

1

Dosage Form

-

Strength

50MG/10ML (5MG/ML)

Approval Date

2025-12-23

Regulatory Status

RX

2023
15 Nov
RX Application: 216007

Drug Name

NALMEFENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Approval Date

2023-11-15

216007 / 1

Active Ingredient

NALMEFENE HYDROCHLORIDE

Application Number

216007

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

Approval Date

2023-11-15

Regulatory Status

RX

2023
15 Nov
RX Application: 216007

Drug Name

NALMEFENE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE/2ML (EQ 1MG BASE/ML)

Approval Date

2023-11-15

216007 / 2

Active Ingredient

NALMEFENE HYDROCHLORIDE

Application Number

216007

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE/2ML (EQ 1MG BASE/ML)

Approval Date

2023-11-15

Regulatory Status

RX

2024
06 Sep
RX Application: 217548

Drug Name

NICARDIPINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/10ML (2.5MG/ML)

Approval Date

2024-09-06

217548 / 1

Active Ingredient

NICARDIPINE HYDROCHLORIDE

Application Number

217548

Product Number

1

Dosage Form

-

Strength

25MG/10ML (2.5MG/ML)

Approval Date

2024-09-06

Regulatory Status

RX

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Drug Status Breakdown
4 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

METHYLENE BLUE

Application Number

219550

Product Number

1

Active Ingredient

METHYLENE BLUE

Dosage Form

-

Strength

50MG/10ML (5MG/ML)

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

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