Naproxen Sodium

Product NDC
76420-627
11-digit product format
764200627
Labeler code
76420
Product ID
76420-627_07f76fa9-dba3-997b-e063-6294a90a6dd5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA212199
Marketing category
ANDA
Marketing start
2019-10-30
Substance
NAPROXEN SODIUM
Active strength
550 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
9TN87S3A3CNAPROXEN SODIUM26159-34-2NAPROXEN SODIUM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-627-0176420062701100 TABLET in 1 BOTTLE (76420-627-01) 100 tablet2023-10-18NoNoHistorical
76420-627-307642006273030 TABLET in 1 BOTTLE (76420-627-30) 30 tablet2023-10-18NoNoHistorical
76420-627-607642006276060 TABLET in 1 BOTTLE (76420-627-60) 60 tablet2023-10-18NoNoHistorical
76420-627-907642006279090 TABLET in 1 BOTTLE (76420-627-90) 90 tablet2023-10-18NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Naproxen SodiumAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-10-18HUMAN PRESCRIPTION DRUG LABEL1