Diclofenac Sodium

Product NDC
51021-150
11-digit product format
510210150
Labeler code
51021
Product ID
51021-150_7d4f42aa-5036-2484-e053-2991aa0ad9c4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Sircle Laboratories, LLC
Application
ANDA202769
Marketing category
ANDA
Marketing start
2015-07-08
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
16 mg/mL
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51021-150-05ML - Milliliter51021-150fc2519f1-c7d3-450d-8646-2de96e08df8c12015-12-02