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01 1ABBVIE

02 5MMT

03 1RAFA LABS LTD

04 1US ARMY

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PharmaCompass

01

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2024 ACI Convention
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ATROPINE

Brand Name : ATROPINE

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 2MG SULFATE/0.7ML

Approval Date : 1987-01-30

Application Number : 71295

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie Company Banner

02

2024 ACI Convention
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2024 ACI Convention
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ATROPINE

Brand Name : ATROPEN

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 2MG SULFATE/0.7ML

Approval Date : 1982-01-01

Application Number : 17106

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

2024 ACI Convention
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2024 ACI Convention
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ATROPINE

Brand Name : ATROPEN

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 1MG SULFATE/0.7ML

Approval Date : 2003-06-19

Application Number : 17106

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

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2024 ACI Convention
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ATROPINE

Brand Name : ATROPEN

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 0.5MG SULFATE/0.7ML

Approval Date : 2003-06-19

Application Number : 17106

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

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2024 ACI Convention
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ATROPINE

Brand Name : ATROPEN

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 0.25MG SULFATE/0.3ML

Approval Date : 2004-09-17

Application Number : 17106

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

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2024 ACI Convention
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ATROPINE; PRALIDOXIME CHLORIDE

Brand Name : DUODOTE

Dosage Form : INJECTABLE;INTRAMUSCULAR

Dosage Strength : 2.1MG/0.7ML;600MG/2ML

Approval Date : 2006-09-28

Application Number : 21983

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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07

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2024 ACI Convention
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ATROPINE

Brand Name : ATROPINE (AUTOINJECTOR)

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : EQ 2MG SULFATE/0.7ML (EQ 2MG SULFATE/0.7ML)

Approval Date : 2018-07-09

Application Number : 212319

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

US ARMY

Country
2024 ACI Convention
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US ARMY

Country
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2024 ACI Convention
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ATROPINE; PRALIDOXIME CHLORIDE

Brand Name : ATNAA

Dosage Form : INJECTABLE;INTRAMUSCULAR

Dosage Strength : 2.1MG/0.7ML;600MG/2ML

Approval Date : 2002-01-17

Application Number : 21175

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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