Almaject
FDA Approved Drugs

Almaject

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 RX
  • Total Records 7
  • Latest Approval Date Jun 04, 2024
  • Data Source FDA
  • First Approval Date Jul 24, 1987
All
7
View
Discontinued
6
View
RX
1
View
Company Overview

Company

Almaject

Country

U.S.A

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Company Snapshot

Almaject

44 Whippany Rd. Suite 300 Morristown, NJ 07960

U.S.A

www.almaject.com/ Almaject-CS@almaject.com View on Map
FDA Approved Drug Records ( 7 records )
1987
24 Jul
Discontinued Application: 62800

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1987-07-24

62800 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62800

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1987-07-24

Regulatory Status

Discontinued

1987
24 Jul
Discontinued Application: 62801

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1987-07-24

62801 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62801

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1987-07-24

Regulatory Status

Discontinued

1988
29 Sep
Discontinued Application: 62943

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1988-09-29

62943 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62943

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE/ML

Approval Date

1988-09-29

Regulatory Status

Discontinued

2012
08 Nov
Discontinued Application: 65515

Drug Name

DOXORUBICIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

2012-11-08

65515 / 1

Active Ingredient

DOXORUBICIN HYDROCHLORIDE

Application Number

65515

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

2012-11-08

Regulatory Status

Discontinued

2019
17 May
Discontinued Application: 204817

Drug Name

MELPHALAN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

2019-05-17

204817 / 1

Active Ingredient

MELPHALAN HYDROCHLORIDE

Application Number

204817

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

2019-05-17

Regulatory Status

Discontinued

2024
04 Jun
RX Application: 218771

Drug Name

TERIPARATIDE

Product Number

1

Dosage Form

-

Strength

0.56MG/2.24ML (0.25MG/ML)

Approval Date

2024-06-04

218771 / 1

Active Ingredient

TERIPARATIDE

Application Number

218771

Product Number

1

Dosage Form

-

Strength

0.56MG/2.24ML (0.25MG/ML)

Approval Date

2024-06-04

Regulatory Status

RX

2016
23 Mar
Discontinued Application: 206398

Drug Name

VORICONAZOLE

Product Number

1

Dosage Form

-

Strength

200MG/VIAL

Approval Date

2016-03-23

206398 / 1

Active Ingredient

VORICONAZOLE

Application Number

206398

Product Number

1

Dosage Form

-

Strength

200MG/VIAL

Approval Date

2016-03-23

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

CLINDAMYCIN PHOSPHATE

Application Number

62800

Product Number

1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Dosage Form

-

Strength

EQ 150MG BASE/ML

FDA Approved Drug Data

Approved drug product information

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