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Approved Drug Products containing 60359 listed in the FDA Orange Book. Original Data : FDA Website

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01 3AZURITY

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01

Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
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Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
arrow

Azurity Pharma

Dosage Form : TABLET; ORAL

Proprietary Name : ERYTHROCIN STEARATE

Dosage Strength : EQ 500MG BASE

Approval Date : 1982-01-01

Application Number : 60359

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

02

Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
arrow

Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
arrow

Azurity Pharma

Dosage Form : TABLET; ORAL

Proprietary Name : ERYTHROCIN STEARATE

Dosage Strength : EQ 250MG BASE

Approval Date : 1982-01-01

Application Number : 60359

RX/OTC/DISCN : RX

RLD : No

TE Code :

blank

03

Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
arrow

Brand Name : ERYTHROCIN STEARATE

FNCE 2024
Not Confirmed
arrow

Azurity Pharma

Dosage Form : TABLET; ORAL

Proprietary Name : ERYTHROCIN STEARATE

Dosage Strength : EQ 125MG BASE

Approval Date : 1982-01-01

Application Number : 60359

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank