Diclofenac Sodium Topical Solution

Product NDC
68788-7151
11-digit product format
687887151
Labeler code
68788
Product ID
68788-7151_c0b6b374-e1ac-4f8f-88b4-667ca3395bb9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206715
Marketing category
ANDA
Marketing start
2018-05-09
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
68788-7151-1ML - Milliliter68788-71511058b0f4-30c5-4048-876e-b539898026de12018-08-13