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 1GLAND
06 3HERITAGE PHARMA
07 2HOSPIRA
08 1LUPIN LTD
09 1MSN
10 1QILU PHARM HAINAN
11 3RISING
12 3RUBICON RESEARCH
13 1SAGENT
14 3SANDOZ
15 3TARO
16 1TEVA PARENTERAL
17 3UPSHER SMITH LABS
18 4VALIDUS PHARMS
19 1WEST-WARD PHARMS INT
20 3ZYDUS PHARMS
01 11INJECTABLE;INJECTION
02 33TABLET;ORAL
01 4DISCN
02 40RX
01 40BUMETANIDE
02 4BUMEX
01 40No
02 4Yes
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 :
