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01 4ATROPINE
02 1ATROPINE; PRALIDOXIME CHLORIDE
03 1MIDAZOLAM HYDROCHLORIDE
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01 6MMT
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01 1INJECTABLE;INTRAMUSCULAR
02 5SOLUTION;INTRAMUSCULAR
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01 12.1MG/0.7ML;600MG/2ML
02 1EQ 0.25MG SULFATE/0.3ML
03 1EQ 0.5MG SULFATE/0.7ML
04 1EQ 1MG SULFATE/0.7ML
05 1EQ 2MG SULFATE/0.7ML
06 1EQ 50MG BASE/10ML (EQ 5MG BASE/ML)
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01 6USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR
Brand Name : ATROPEN
Dosage Strength : EQ 2MG SULFATE/0.7ML
Packaging :
Approval Date : 1982-01-01
Application Number : 17106
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR
Brand Name : ATROPEN
Dosage Strength : EQ 1MG SULFATE/0.7ML
Packaging :
Approval Date : 2003-06-19
Application Number : 17106
Regulatory Info : DISCN
Registration Country : USA

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.
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR
Brand Name : ATROPEN
Dosage Strength : EQ 0.5MG SULFATE/0.7ML
Packaging :
Approval Date : 2003-06-19
Application Number : 17106
Regulatory Info : DISCN
Registration Country : USA

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.
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR
Brand Name : ATROPEN
Dosage Strength : EQ 0.25MG SULFATE/0.3M...
Packaging :
Approval Date : 2004-09-17
Application Number : 17106
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
ATROPINE; PRALIDOXIME CHLORIDE
Dosage Form : INJECTABLE;INTRAMUSCULAR
Brand Name : DUODOTE
Dosage Strength : 2.1MG/0.7ML;600MG/2ML
Packaging :
Approval Date : 2006-09-28
Application Number : 21983
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAMUSCULAR
Brand Name : SEIZALAM
Dosage Strength : EQ 50MG BASE/10ML (EQ ...
Packaging :
Approval Date : 2018-09-14
Application Number : 209566
Regulatory Info : DISCN
Registration Country : USA
