NDC 50090-0747

Nabumetone

Nabumetone

Nabumetone is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Nabumetone.

Product ID50090-0747_162a69c0-ff0b-423b-9b11-6977c7852e82
NDC50090-0747
Product TypeHuman Prescription Drug
Proprietary NameNabumetone
Generic NameNabumetone
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-06-13
Marketing CategoryANDA / ANDA
Application NumberANDA091083
Labeler NameA-S Medication Solutions
Substance NameNABUMETONE
Active Ingredient Strength500 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 50090-0747-0

60 TABLET, FILM COATED in 1 BOTTLE (50090-0747-0)
Marketing Start Date2014-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-0747-0 [50090074700]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-18
Marketing End Date2017-10-18

NDC 50090-0747-7 [50090074707]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-18
Marketing End Date2017-10-18

NDC 50090-0747-4 [50090074704]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-18
Marketing End Date2017-10-18

NDC 50090-0747-5 [50090074705]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-18
Marketing End Date2017-10-18

NDC 50090-0747-2 [50090074702]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-28
Marketing End Date2016-07-31

NDC 50090-0747-8 [50090074708]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091083
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-18
Marketing End Date2017-10-18

Drug Details

NDC Crossover Matching brand name "Nabumetone" or generic name "Nabumetone"

NDCBrand NameGeneric Name
0115-1657NabumetoneNabumetone
0115-1658NabumetoneNabumetone
0185-0145NabumetoneNabumentone
0185-0146NabumetoneNabumentone
0440-5843NabumetoneNabumetone
0440-5844NabumetoneNabumetone
0591-3670NabumetoneNabumetone
0591-3671NabumetoneNabumetone
0615-7630Nabumetonenabumetone
0615-7645Nabumetonenabumetone
0615-7666NabumetoneNabumetone
0615-7667NabumetoneNabumetone
10544-003NabumetoneNabumetone
10544-120NabumetoneNabumetone
10544-271NabumetoneNabumetone
10544-273NabumetoneNabumetone
21695-230NabumetoneNabumetone
21695-231NabumetoneNabumetone
33261-077NabumetoneNabumetone
33261-078NabumetoneNabumetone
33358-251NabumetoneNabumetone
33358-252NabumetoneNabumetone
35356-685NabumetoneNabumentone
35356-686NabumetoneNabumetone
35356-687NabumetoneNabumetone
35356-726NabumetoneNabumetone
68084-051NabumetoneNabumetone
68151-0574NabumetoneNabumetone
68180-142NabumetoneNabumetone
68180-141NabumetoneNabumetone
68462-359NabumetoneNabumetone
68462-358NabumetoneNabumetone
68788-7220NabumetoneNabumetone
68788-9909NabumetoneNabumetone
68788-9908NabumetoneNabumetone
69097-965NabumetoneNabumetone
69097-966NabumetoneNabumetone
70518-0934NabumetoneNabumetone
70518-0614NabumetoneNabumetone
70518-0698NabumetoneNabumetone
70934-013NabumetoneNabumetone
71205-030NabumetoneNabumetone
71335-0781NabumetoneNabumetone
71335-0531NabumetoneNabumetone
71335-0754NabumetoneNabumetone
71335-0939NabumetoneNabumetone
76282-258NabumetoneNabumetone
76282-257NabumetoneNabumetone
43063-859NabumetoneNabumetone
45865-351NabumetoneNabumetone
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