HQ SPCLT PHARMA Discontinued
FDA Approved Drugs

HQ SPCLT PHARMA Discontinued

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.

Discontinued
  • Total Records 4
  • Latest Approval Date Dec 14, 2020
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
37
View
Discontinued
4
View
RX
33
View
Company Overview

Company

HQ SPCLT PHARMA Discontinued

Country

U.S.A

Website

Email

Social Profiles

Company Snapshot

HQ SPCLT PHARMA Discontinued

U.S.A

View on Map
FDA Approved Drug Records ( 4 records )
2020
14 Dec
Discontinued Application: 202543

Drug Name

LEVETIRACETAM IN SODIUM CHLORIDE

Product Number

4

Dosage Form

-

Strength

250MG/50ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2020-12-14

202543 / 4

Active Ingredient

LEVETIRACETAM

Application Number

202543

Product Number

4

Dosage Form

-

Strength

250MG/50ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2020-12-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18057

Drug Name

PLATINOL

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1982-01-01

18057 / 1

Active Ingredient

CISPLATIN

Application Number

18057

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
18 Jul
Discontinued Application: 18057

Drug Name

PLATINOL-AQ

Product Number

3

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1984-07-18

18057 / 3

Active Ingredient

CISPLATIN

Application Number

18057

Product Number

3

Dosage Form

-

Strength

0.5MG/ML

Approval Date

1984-07-18

Regulatory Status

Discontinued

1992
29 Dec
Discontinued Application: 20262

Drug Name

TAXOL

Product Number

1

Dosage Form

-

Strength

6MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-12-29

20262 / 1

Active Ingredient

PACLITAXEL

Application Number

20262

Product Number

1

Dosage Form

-

Strength

6MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-12-29

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    37 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
4 total
  • 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

LEVETIRACETAM IN SODIUM CHLORIDE

Application Number

202543

Product Number

4

Active Ingredient

LEVETIRACETAM

Dosage Form

-

Strength

250MG/50ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.