Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

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01 3MANKIND PHARMA
02 3AMNEAL PHARMS CO
03 1ANTHEA PHARMA
04 3APPCO
05 1ASPIRO
06 1CORSTASIS THERAP
07 1GLAND
08 3HERITAGE PHARMA
09 2HOSPIRA
10 3JUBILANT GENERICS
11 1LUPIN LTD
12 4MSN
13 1QILU PHARM HAINAN
14 3RISING
15 3RUBICON RESEARCH
16 1SAGENT
17 3SANDOZ
18 3TARO
19 1TEVA PARENTERAL
20 3UPSHER SMITH LABS
21 4VALIDUS PHARMS
22 1WEST-WARD PHARMS INT
23 3ZYDUS PHARMS
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01 12INJECTABLE;INJECTION
02 1SPRAY;NASAL
03 39TABLET;ORAL
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01 4DISCN
02 48RX
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01 47BUMETANIDE
02 4BUMEX
03 1ENBUMYST
01 47No
02 5Yes
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BUMETANIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 2025-04-03
Application Number : 219291
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BUMETANIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Approval Date : 2025-04-03
Application Number : 219291
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BUMETANIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG
Approval Date : 2025-04-03
Application Number : 219291
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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RLD : No
TE Code : AB
Brand Name : BUMETANIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 1995-04-24
Application Number : 74225
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Brand Name : BUMETANIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Approval Date : 1995-04-24
Application Number : 74225
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code :
Brand Name : BUMETANIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.25MG/ML
Approval Date : 1997-10-30
Application Number : 74160
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code : AB
Brand Name : BUMEX
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Approval Date : 1983-02-28
Application Number : 18225
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code : AB
Brand Name : BUMEX
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 1983-02-28
Application Number : 18225
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code : AB
Brand Name : BUMEX
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG
Approval Date : 1985-06-14
Application Number : 18225
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code :
Brand Name : BUMEX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-02-28
Application Number : 18226
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
