DICLOFENAC SODIUM

Product NDC
63629-8644
11-digit product format
636298644
Labeler code
63629
Product ID
63629-8644_fa655edf-b1bf-405c-b76b-b0a9aee0cd50
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diclofenac sodium
Dosage form
GEL
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA211253
Marketing category
ANDA
Marketing start
2019-05-20
Marketing end
0000-00-00
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-8644-1GM - Gram63629-86440f9c8f81-e807-4ead-a467-8bd14ba8274c12021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-8644-1636298644011 TUBE in 1 CARTON (63629-8644-1) > 100 g in 1 TUBE1 tube2019-05-200000-00-00NoNoCurrent