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01 1CITALOPRAM HYDROBROMIDE
02 3DULOXETINE HYDROCHLORIDE
03 1ESCITALOPRAM OXALATE
04 5GABAPENTIN
05 3HYDROCHLOROTHIAZIDE; LISINOPRIL
06 4LORAZEPAM
07 3NITROFURANTOIN, MACROCRYSTALLINE
08 1NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
09 2SERTRALINE HYDROCHLORIDE
10 1VENLAFAXINE BESYLATE
11 1ZOLPIDEM TARTRATE
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01 25ALMATICA
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01 3CAPSULE, DELAYED REL PELLETS;ORAL
02 4CAPSULE, EXTENDED RELEASE;ORAL
03 9CAPSULE;ORAL
04 1TABLET, EXTENDED RELEASE;ORAL
05 8TABLET;ORAL
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01 11.5MG
02 1100MG
03 112.5MG;10MG
04 112.5MG;20MG
05 11MG
06 125MG
07 125MG;20MG
08 12MG
09 1300MG
10 13MG
11 1450MG
12 150MG
13 1600MG
14 17.5MG
15 1750MG
16 175MG;25MG
17 1900MG
18 1EQ 112.5MG BASE
19 1EQ 120MG BASE
20 1EQ 150MG BASE
21 1EQ 15MG BASE
22 1EQ 200MG BASE
23 1EQ 30MG BASE
24 1EQ 80MG BASE
25 1EQ 90MG BASE
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01 25USA
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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CITALOPRAM HYDROBROMIDE
Dosage Strength : EQ 30MG BASE
Packaging :
Approval Date : 2022-01-31
Application Number : 215428
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 80MG BASE
Packaging :
Approval Date : 2026-02-27
Application Number : 219131
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 90MG BASE
Packaging :
Approval Date : 2026-02-27
Application Number : 219131
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 120MG BASE
Packaging :
Approval Date : 2026-02-27
Application Number : 219131
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : ESCITALOPRAM
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 2025-08-29
Application Number : 219130
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GRALISE
Dosage Strength : 300MG
Packaging :
Approval Date : 2011-01-28
Application Number : 22544
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GRALISE
Dosage Strength : 600MG
Packaging :
Approval Date : 2011-01-28
Application Number : 22544
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GRALISE
Dosage Strength : 450MG
Packaging :
Approval Date : 2023-04-18
Application Number : 22544
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GRALISE
Dosage Strength : 750MG
Packaging :
Approval Date : 2023-04-18
Application Number : 22544
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GRALISE
Dosage Strength : 900MG
Packaging :
Approval Date : 2023-04-18
Application Number : 22544
Regulatory Info : RX
Registration Country : USA

Almatica Pharma Inc is a supplier offers 3 products (APIs, Excipients or Intermediates).
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