NDC 79739-7078

Nabumetone 1000 mg

Nabumetone

Nabumetone 1000 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Lgm Pharma Solutions, Llc. The primary component is Nabumetone.

Product ID79739-7078_5c377fe9-b436-4f31-9b90-0208d8bc407f
NDC79739-7078
Product TypeHuman Prescription Drug
Proprietary NameNabumetone 1000 mg
Generic NameNabumetone
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-09-04
Marketing CategoryANDA / ANDA
Application NumberANDA203166
Labeler NameLGM Pharma Solutions, LLC
Substance NameNABUMETONE
Active Ingredient Strength1000 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 79739-7078-1

100 TABLET, FILM COATED in 1 BOTTLE (79739-7078-1)
Marketing Start Date2019-09-04
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Nabumetone 1000 mg" or generic name "Nabumetone"

NDCBrand NameGeneric Name
0722-7078Nabumetone 1000 mgNabumetone
79739-7078Nabumetone 1000 mgNabumetone 1000 mg
0115-1657NabumetoneNabumetone
0115-1658NabumetoneNabumetone
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
35356-686NabumetoneNabumetone
35356-687NabumetoneNabumetone
35356-726NabumetoneNabumetone
43063-859NabumetoneNabumetone
0722-7076Nabumetone 500 mgNabumetone
0722-7077Nabumetone 750 mgNabumetone
15370-170RELAFEN DSNABUMETONE

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