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01 3Bosutinib
02 1CALCIUM ACETATE
03 1Dydrogesterone
04 6LENALIDOMIDE
05 6LEVETIRACETAM
06 1LEVONORGESTREL
07 1METHOTREXATE SODIUM
08 1MIDOSTAURIN
09 2NINTEDANIB
10 4Nintedanib
11 3PARICALCITOL
12 4Pomalidomide
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01 21LOTUS PHARM CO LTD
02 12LOTUS PHARMA BULGARIA EOOD
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01 13CAPSULE;ORAL
02 4Film Coated Tablet
03 4Hard Capsule
04 4Soft Capsule
05 2TABLET, EXTENDED RELEASE;ORAL
06 6TABLET;ORAL
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01 10.75MG
02 4100MG
03 210MG
04 3150MG
05 115MG
06 11GM
07 11MCG
08 11MG
09 12.5MG
10 120MG
11 1250MG
12 225MG
13 12MCG
14 12MG
15 13MG
16 1400MG
17 14MCG
18 14MG
19 3500MG
20 15MG
21 1667MG
22 2750MG
23 1EQ 2.5MG BASE
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01 12Malta
02 21USA
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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Bosutinib Lotus
Dosage Strength : 100MG
Packaging :
Approval Date : 2025-02-14
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Bosutinib Lotus
Dosage Strength : 400MG
Packaging :
Approval Date : 2025-02-14
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Bosutinib Lotus
Dosage Strength : 500MG
Packaging :
Approval Date : 2025-02-14
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : CALCIUM ACETATE
Dosage Strength : 667MG
Packaging :
Approval Date : 2016-07-26
Application Number : 203298
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Dydrogesterone Lotus
Dosage Strength : 10MG
Packaging :
Approval Date : 2024-12-03
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : LENALIDOMIDE
Dosage Strength : 5MG
Packaging :
Approval Date : 2022-08-31
Application Number : 210480
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : LENALIDOMIDE
Dosage Strength : 10MG
Packaging :
Approval Date : 2022-08-31
Application Number : 210480
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : LENALIDOMIDE
Dosage Strength : 15MG
Packaging :
Approval Date : 2022-08-31
Application Number : 210480
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : LENALIDOMIDE
Dosage Strength : 25MG
Packaging :
Approval Date : 2022-08-31
Application Number : 210480
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : LENALIDOMIDE
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2023-03-06
Application Number : 210480
Regulatory Info : RX
Registration Country : USA

Lotus Pharmaceutical is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of TM-1 (N-[2-(2-METHOXYPHENOXY)ETHYL]NORGLAUCINE) bulk offered by Lotus Pharmaceutical