Diclofenac Sodium

Product NDC
60760-789
11-digit product format
607600789
Labeler code
60760
Product ID
60760-789_7a7fe880-0c08-015c-e053-2991aa0a02bb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA074394
Marketing category
ANDA
Marketing start
1995-11-30
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
75 mg/1
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60760-789-10EA - Each60760-789c3fc08d4-7ff4-451b-adc0-8e8aefac169212017-06-15
60760-789-15EA - Each60760-789b9666a25-6341-4b96-b54e-c8c51eb7033f12017-06-15
60760-789-20EA - Each60760-7899101e564-0155-490e-b693-892a671fcbd512017-06-15
60760-789-60EA - Each60760-789367afbdc-03df-4f21-b5a6-e60c81176de312017-06-15