VOLTAREN ARTHRITIS PAIN

Product NDC
50090-6202
11-digit product format
500906202
Labeler code
50090
Product ID
50090-6202_46659e9a-60dd-4637-8aa4-561c48722736
Type
HUMAN OTC DRUG
Nonproprietary name
diclofenac sodium
Dosage form
GEL
Route
TOPICAL
Labeler
A-S Medication Solutions
Application
NDA022122
Marketing category
NDA
Marketing start
2020-05-13
Substance
DICLOFENAC SODIUM
Active strength
10 mg/g
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], 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
QTG126297QDICLOFENAC SODIUM15307-79-6DICLOFENAC SODIUM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50090-6202-05009062020024 TUBE in 1 CASE (50090-6202-0) / 50 g in 1 TUBE24 tube2022-11-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
VOLTAREN ARTHRITIS PAINA-S Medication Solutions2024-05-30HUMAN OTC DRUG LABEL2