Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 3MANKIND PHARMA
02 3AMNEAL PHARMS CO
03 3APPCO
04 1ASPIRO
05 1CORSTASIS THERAPEUTICS
06 1GLAND
07 3HERITAGE PHARMA
08 2HOSPIRA
09 3JUBILANT GENERICS
10 1LUPIN LTD
11 1MSN
12 1QILU PHARM HAINAN
13 3RISING
14 3RUBICON RESEARCH
15 1SAGENT
16 3SANDOZ
17 3TARO
18 1TEVA PARENTERAL
19 3UPSHER SMITH LABS
20 4VALIDUS PHARMS
21 1WEST-WARD PHARMS INT
22 3ZYDUS PHARMS
01 11INJECTABLE;INJECTION
02 1SPRAY;NASAL
03 36TABLET;ORAL
01 4DISCN
02 43RX
03 1Blank
01 43BUMETANIDE
02 4BUMEX
03 1ENBUMYST
01 43No
02 4Yes
03 1Blank
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
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
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
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 :
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
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
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
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 :
