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

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01 2BAYER HLTHCARE

02 2LUPIN LTD

03 2WATSON LABS INC

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PharmaCompass

01

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.02MG,N/A;0.451MG,0.451MG

Approval Date : 2016-10-11

Application Number : 203593

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.03MG,N/A;0.451MG,0.451MG

Approval Date : 2016-10-11

Application Number : 203594

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : BEYAZ

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.02MG,N/A;0.451MG,0.451MG

Approval Date : 2010-09-24

Application Number : 22532

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : SAFYRAL

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.03MG,N/A;0.451MG,0.451MG

Approval Date : 2010-12-16

Application Number : 22574

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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05

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.02MG,N/A;0.451MG,0.451MG

Approval Date : 2018-06-13

Application Number : 205947

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

DROSPIRENONE; ETHINYL ESTRADIOL; LEVOMEFOLATE CALCIUM

Brand Name : TYDEMY

Dosage Form : TABLET;ORAL

Dosage Strength : 3MG,N/A;0.03MG,N/A;0.451MG,0.451MG

Approval Date : 2017-12-12

Application Number : 205948

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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