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01 1Dr. Reddy's Laboratories

02 12care4

03 4Accord healthcare

04 1Almaject

05 1Alvogen

06 1AmbioPharm

07 1Amphastar Pharmaceuticals

08 2Apotex Inc

09 1Avir Pharma

10 2CinnaGen

11 1Cipla Medpro South Africa

12 10Eli Lilly

13 1Eurogenerics Holdings Bv

14 1Future Health Pharma Gmbh

15 1GP Pharm

16 14Gedeon Richter

17 4Generic Health

18 1Italfarmaco S.p.A

19 1Mepha Pharma

20 1Neopharmed Gentili

21 2ORIFARM GROUP AS

22 7STADA Arzneimittel

23 1Savior Lifetec Corporation

24 1Spirig Healthcare

25 2Sun Pharmaceutical Industries Limited

26 5Teva Pharmaceutical Industries

27 2Theramex

28 1Welding GmbH & Co.KG

29 1Zentiva

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Teriparatide

Brand Name :

Dosage Form : Injection

Dosage Strength : 0.25MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

02

VMX
Not Confirmed
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VMX
Not Confirmed

Teriparatid

Brand Name : Sondelbay

Dosage Form : Solution For Injection

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 24/03/2022

Application Number : 20210306000046

Regulatory Info : Approved

Registration Country : Sweden

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03

VMX
Not Confirmed
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VMX
Not Confirmed

TERIPARATIDE

Brand Name : TERIPARATIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date : 2024-06-04

Application Number : 218771

Regulatory Info : RX

Registration Country : USA

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04

VMX
Not Confirmed
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Not Confirmed

TERIPARATIDE

Brand Name : BONSITY

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date : 2019-10-04

Application Number : 211939

Regulatory Info : RX

Registration Country : USA

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05

VMX
Not Confirmed
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VMX
Not Confirmed

TERIPARATIDE

Brand Name : TERIPARATIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date :

Application Number : 213641

Regulatory Info :

Registration Country : USA

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06

VMX
Not Confirmed
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VMX
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TERIPARATIDE

Brand Name : TERIPARATIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date : 2023-11-16

Application Number : 211097

Regulatory Info : RX

Registration Country : USA

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07

VMX
Not Confirmed
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Teriparatide

Brand Name : CinnoPar

Dosage Form : Injectable

Dosage Strength : 250MCG/ML

Packaging : Vial/Pen

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Iran

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08

VMX
Not Confirmed
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TERIPARATIDE

Brand Name : FORTEO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.75MG/3ML (0.25MG/ML)

Packaging :

Approval Date : 2002-11-26

Application Number : 21318

Regulatory Info : DISCN

Registration Country : USA

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09

VMX
Not Confirmed
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VMX
Not Confirmed

TERIPARATIDE

Brand Name : FORTEO

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date : 2008-06-25

Application Number : 21318

Regulatory Info : RX

Registration Country : USA

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10

VMX
Not Confirmed
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Teriparatide

Brand Name : FORSTEO

Dosage Form : Solution For Injection In Pre-Filled Pen

Dosage Strength : 20 mcg/80 mcl

Packaging : 1 UNIT 20 MCG/80 MCL - PARENTERAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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11

VMX
Not Confirmed
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Teriparatid

Brand Name : Forsteo

Dosage Form : Solution For Injection

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 10/06/2003

Application Number : 20030610000019

Regulatory Info : Approved

Registration Country : Sweden

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12

VMX
Not Confirmed
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Not Confirmed

Teriparatid

Brand Name : Terrosa

Dosage Form : Injectable Solution

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 04/01/2017

Application Number : 20151204000052

Regulatory Info : Approved

Registration Country : Sweden

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13

VMX
Not Confirmed
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VMX
Not Confirmed

Teriparatid

Brand Name : Terrosa

Dosage Form : Solution For Injection

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 23/08/2023

Application Number : 20230817000014

Regulatory Info : Approved

Registration Country : Sweden

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14

VMX
Not Confirmed
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Not Confirmed

Teriparatide

Brand Name : OSEFFYL

Dosage Form : Solution For Injection In Pre-Filled Pen

Dosage Strength : 20 micrograms/80 microliters

Packaging : 1 UNIT 20 MCG/80 MCL - PARENTERAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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15

VMX
Not Confirmed
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Not Confirmed

Teriparatide

Brand Name : PATRIDE

Dosage Form : Solution For Injection In Pre-Filled Pen

Dosage Strength : 20 micrograms/80 microliters

Packaging : 1 UNIT 20 MCG/80 MCL - PARENTERAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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16

VMX
Not Confirmed
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Teriparatide

Brand Name :

Dosage Form :

Dosage Strength :

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Taiwan

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17

VMX
Not Confirmed
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Teriparatid

Brand Name : Movymia

Dosage Form : Injectable Solution

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 11/01/2017

Application Number : 20151204000069

Regulatory Info : Approved

Registration Country : Sweden

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18

VMX
Not Confirmed
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TERIPARATIDE

Brand Name : TERIPARATIDE

Dosage Form : SOLUTION;SUBCUTANEOUS

Dosage Strength : 0.56MG/2.24ML (0.25MG/ML)

Packaging :

Approval Date : 2023-11-16

Application Number : 208569

Regulatory Info : RX

Registration Country : USA

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19

VMX
Not Confirmed
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Not Confirmed

Teriparatide

Brand Name : TERIPARATIDE TEVA

Dosage Form : Solution For Injection In Pre-Filled Pen

Dosage Strength : 20 micrograms/80 microliters

Packaging : 1 UNIT 20 MCG/80 MCL - PARENTERAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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20

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Teriparatid

Brand Name : Livogiva

Dosage Form : Solution For Injection

Dosage Strength : 20mcg/80mikroliter

Packaging :

Approval Date : 27/08/2020

Application Number : 20190507000031

Regulatory Info : Approved

Registration Country : Sweden

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