Naproxen

Product NDC
71335-2485
11-digit product format
713352485
Labeler code
71335
Product ID
71335-2485_7f075beb-f2b7-40e2-a4f4-a220bf1a2ac7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078250
Marketing category
ANDA
Marketing start
2007-07-01
Substance
NAPROXEN
Active strength
500 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
57Y76R9ATQNAPROXEN22204-53-1NAPROXEN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2485-07133524850028 TABLET in 1 BOTTLE (71335-2485-0) 28 tablet2024-09-03NoNoHistorical
71335-2485-17133524850130 TABLET in 1 BOTTLE (71335-2485-1) 30 tablet2024-09-03NoNoHistorical
71335-2485-27133524850260 TABLET in 1 BOTTLE (71335-2485-2) 60 tablet2024-09-03NoNoHistorical
71335-2485-37133524850310 TABLET in 1 BOTTLE (71335-2485-3) 10 tablet2024-09-03NoNoHistorical
71335-2485-47133524850490 TABLET in 1 BOTTLE (71335-2485-4) 90 tablet2024-09-03NoNoHistorical
71335-2485-57133524850520 TABLET in 1 BOTTLE (71335-2485-5) 20 tablet2024-09-03NoNoHistorical
71335-2485-671335248506120 TABLET in 1 BOTTLE (71335-2485-6) 120 tablet2024-09-03NoNoHistorical
71335-2485-77133524850714 TABLET in 1 BOTTLE (71335-2485-7) 14 tablet2024-09-03NoNoHistorical
71335-2485-87133524850842 TABLET in 1 BOTTLE (71335-2485-8) 42 tablet2024-09-03NoNoHistorical
71335-2485-97133524850940 TABLET in 1 BOTTLE (71335-2485-9) 40 tablet2024-09-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NaproxenBryant Ranch Prepack2024-09-03HUMAN PRESCRIPTION DRUG LABEL1