HOPE PHARMS
FDA Approved Drugs

HOPE PHARMS

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 3
  • Latest Approval Date Feb 14, 2012
  • Data Source FDA
  • First Approval Date Jan 14, 2011
Company Overview

Company

HOPE PHARMS

Country

U.S.A

Website

Email

questions@hopepharm.com

Social Profiles

Company Snapshot

HOPE PHARMS

Hope Pharmaceuticals 16416 N

U.S.A

questions@hopepharm.com View on Map
FDA Approved Drug Records ( 3 records )
2011
14 Jan
RX Application: 201444

Drug Name

NITHIODOTE

Product Number

1

Dosage Form

-

Strength

300MG/10ML(30MG/ML),N/A;N/A,12.5GM/50ML(250MG/ML)

Approval Date

2011-01-14

201444 / 1

Active Ingredient

SODIUM NITRITE; SODIUM THIOSULFATE

Application Number

201444

Product Number

1

Dosage Form

-

Strength

300MG/10ML(30MG/ML),N/A;N/A,12.5GM/50ML(250MG/ML)

Approval Date

2011-01-14

Regulatory Status

RX

2012
14 Feb
RX Application: 203922

Drug Name

SODIUM NITRITE

Product Number

1

Dosage Form

-

Strength

300MG/10ML (30MG/ML)

Approval Date

2012-02-14

203922 / 1

Active Ingredient

SODIUM NITRITE

Application Number

203922

Product Number

1

Dosage Form

-

Strength

300MG/10ML (30MG/ML)

Approval Date

2012-02-14

Regulatory Status

RX

2012
14 Feb
RX Application: 203923

Drug Name

SODIUM THIOSULFATE

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML (250MG/ML)

Approval Date

2012-02-14

203923 / 1

Active Ingredient

SODIUM THIOSULFATE

Application Number

203923

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML (250MG/ML)

Approval Date

2012-02-14

Regulatory Status

RX

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Drug Status Breakdown
3 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

NITHIODOTE

Application Number

201444

Product Number

1

Active Ingredient

SODIUM NITRITE; SODIUM THIOSULFATE

Dosage Form

-

Strength

300MG/10ML(30MG/ML),N/A;N/A,12.5GM/50ML(250MG/ML)

FDA Approved Drug Data

Approved drug product information

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