LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 3LGM PHARMA
02 2ANNORA PHARMA
03 2AUROBINDO PHARMA USA
04 2CHARTWELL MOLECULES
05 2CHARTWELL RX
06 1COPLEY PHARM
07 2EPIC PHARMA LLC
08 2IMPAX LABS INC
09 2INVAGEN PHARMS
10 2NOSTRUM LABS INC
11 2OXFORD PHARMS
12 2SCIEGEN PHARMS INC
13 2SMITHKLINE BEECHAM
14 2WATSON LABS
01 28TABLET;ORAL
01 13DISCN
02 15RX
01 26NABUMETONE
02 2RELAFEN
01 26No
02 2Yes
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
RLD : No
TE Code : AB
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2019-08-30
Application Number : 203166
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
RLD : No
TE Code : AB
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Approval Date : 2019-08-30
Application Number : 203166
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
RLD : No
TE Code :
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 1GM
Approval Date : 2019-08-30
Application Number : 203166
RX/OTC/DISCN : RX
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2002-02-25
Application Number : 75280
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Approval Date : 2002-02-25
Application Number : 75280
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Approval Date : 2000-06-06
Application Number : 75179
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : RELAFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-12-24
Application Number : 19583
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : RELAFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-12-24
Application Number : 19583
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2000-05-26
Application Number : 75189
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : NABUMETONE
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG
Approval Date : 2001-09-24
Application Number : 75189
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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