HQ SPECLT PHARMA
FDA Approved Drugs

HQ SPECLT PHARMA

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 Discontinued

Total Records 16
Latest Approval Date Jul 23, 2009
Data Source FDA
First Approval Date Jul 14, 1992

All

View

Discontinued

View

Company Overview

Company

HQ SPECLT PHARMA

Country

U.S.A

Website

Social Profiles

Company Snapshot

HQ SPECLT PHARMA

U.S.A

View on Map

FDA Approved Drug Records ( 16 records )

2005

30 Nov

RX Application: 65176

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2005-11-30

65176 / 1 View Details

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65176

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2005-11-30

Regulatory Status

2005

30 Nov

RX Application: 65176

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2005-11-30

65176 / 2 View Details

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65176

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2005-11-30

Regulatory Status

2005

25 Nov

RX Application: 65188

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL

Approval Date

2005-11-25

65188 / 1 View Details

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65188

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL

Approval Date

2005-11-25

Regulatory Status

1993

15 Apr

RX Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1993-04-15

62772 / 1 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

1993

15 Apr

Discontinued Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1993-04-15

62772 / 2 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

Discontinued

1993

15 Apr

RX Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-04-15

62772 / 3 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

1993

15 Apr

Discontinued Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-04-15

62772 / 4 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

Discontinued

1993

15 Apr

Discontinued Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 125MG BASE/VIAL

Approval Date

1993-04-15

62772 / 5 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 125MG BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

Discontinued

1993

15 Apr

RX Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 250MG BASE/VIAL

Approval Date

1993-04-15

62772 / 6 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 250MG BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

1993

15 Apr

RX Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1993-04-15

62772 / 7 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

1993

15 Apr

Discontinued Application: 62772

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1993-04-15

62772 / 8 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

62772

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

Discontinued

1993

15 Apr

RX Application: 63142

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1993-04-15

63142 / 1 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

63142

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1993-04-15

Regulatory Status

2009

23 Jul

RX Application: 65149

Drug Name

PENICILLIN G POTASSIUM

Product Number

Dosage Form

Strength

1,000,000 UNITS/VIAL

Approval Date

2009-07-23

65149 / 1 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

65149

Product Number

Dosage Form

Strength

1,000,000 UNITS/VIAL

Approval Date

2009-07-23

Regulatory Status

2009

23 Jul

RX Application: 65149

Drug Name

PENICILLIN G POTASSIUM

Product Number

Dosage Form

Strength

5,000,000 UNITS/VIAL

Approval Date

2009-07-23

65149 / 2 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

65149

Product Number

Dosage Form

Strength

5,000,000 UNITS/VIAL

Approval Date

2009-07-23

Regulatory Status

2009

23 Jul

RX Application: 65149

Drug Name

PENICILLIN G POTASSIUM

Product Number

Dosage Form

Strength

20,000,000 UNITS/VIAL

Approval Date

2009-07-23

65149 / 3 View Details

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

65149

Product Number

Dosage Form

Strength

20,000,000 UNITS/VIAL

Approval Date

2009-07-23

Regulatory Status

1992

14 Jul

Discontinued Application: 20119

Drug Name

VUMON

Product Number

Dosage Form

Strength

10MG/ML

Approval Date

1992-07-14

20119 / 1 View Details

Active Ingredient

TENIPOSIDE

Application Number

20119

Product Number

Dosage Form

Strength

10MG/ML

Approval Date

1992-07-14

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
16 View
Drug Prices in Switzerland
0 View

Drug Status Breakdown

16 total

RX
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

AMPICILLIN AND SULBACTAM

Application Number

65176

Product Number

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Dosage Form

Strength

EQ 1GM BASE/VIAL;EQ 500MG 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

Create a New Buying Request

Fields marked with * are mandatory.

Required Quantity *

Please enter quantity.

Measurement Unit *

Please select a unit.

Quality Standard *

Please select quality standard.

Request Type *

Please select request type.

Product Specifications *

Please provide product specifications.

Additional Details *

Please enter additional details.

Shipping Preference *

Please select shipping preference.

Expected Delivery Date

Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.