Almaject RX
FDA Approved Drugs

Almaject 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 1
  • Latest Approval Date Jun 04, 2024
  • Data Source FDA
  • First Approval Date Jun 04, 2024
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7
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Discontinued
6
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RX
1
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Company Overview

Company

Almaject RX

Country

U.S.A

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Almaject RX

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 ( 1 record )
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

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Drug Status Breakdown
1 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

TERIPARATIDE

Application Number

218771

Product Number

1

Active Ingredient

TERIPARATIDE

Dosage Form

-

Strength

0.56MG/2.24ML (0.25MG/ML)

FDA Approved Drug Data

Approved drug product information

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