Signature Care Naproxen Sodium

Product NDC
21130-187
11-digit product format
211300187
Labeler code
21130
Product ID
21130-187_38392888-1e16-49ee-b149-2217936330b4
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Safeway
Application
ANDA074661
Marketing category
ANDA
Marketing start
2021-06-29
Marketing end
0000-00-00
Substance
NAPROXEN SODIUM
Active strength
220 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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-187SIGNATURE CARE NAPROXEN SODIUM (NAPROXEN SODIUM) TABLET, FILM COATED [SAFEWAY]4Legacy NDC20250316_3703ee78-695e-4638-90aa-3ce57a65757e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21130-187-71211300187711 BOTTLE in 1 CARTON (21130-187-71) > 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2021-06-290000-00-00NoNoCurrent
21130-187-75211300187751 BOTTLE in 1 CARTON (21130-187-75) > 90 TABLET, FILM COATED in 1 BOTTLE1 bottle2022-04-070000-00-00NoNoCurrent
21130-187-78211300187781 BOTTLE in 1 CARTON (21130-187-78) > 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2021-06-290000-00-00NoNoCurrent