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Approved Drug Products containing 21367 listed in the FDA Orange Book. Original Data : FDA Website

FDA Orange Book

EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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Bora Pharmaceuticals- Making success more certain.

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Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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Axplora- The partner of choice for complex APIs.

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Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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filter Applicant Reset all filters

2 All

01 2MILLICENT

filter Dosage Reset all filters

2 All

01 2INSERT, EXTENDED RELEASE;VAGINAL

filter Regulatory Info Reset all filters

2 All

01 2RX

filter Brand Name Reset all filters

2 All

01 2FEMRING

filter RLD Reset all filters

2 All

01 2Yes

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Brand Name : FEMRING

Luxepack

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Brand Name : FEMRING

Luxepack

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

RLD : Yes

TE Code :

ESTRADIOL ACETATE

Dosage Form : INSERT, EXTENDED RELEASE; VAGI...

Proprietary Name : FEMRING

Dosage Strength : EQ 0.05MG BASE/24HR

Approval Date : 2003-03-20

Application Number : 21367

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
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02

Brand Name : FEMRING

Luxepack

Not Confirmed

Brand Name : FEMRING

Luxepack

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

RLD : Yes

TE Code :

ESTRADIOL ACETATE

Dosage Form : INSERT, EXTENDED RELEASE; VAGI...

Proprietary Name : FEMRING

Dosage Strength : EQ 0.1MG BASE/24HR

Approval Date : 2003-03-20

Application Number : 21367

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
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Stock Recap
#PipelineProspector

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Place

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