Diclofenac Sodium

Product NDC
43063-693
11-digit product format
430630693
Labeler code
43063
Product ID
43063-693_7d4f5b39-d094-5353-e053-2a91aa0a8db9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diclofenac Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA075185
Marketing category
ANDA
Marketing start
1998-11-13
Marketing end
0000-00-00
Substance
DICLOFENAC SODIUM
Active strength
50 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
43063-693-60EA - Each43063-69359c64b3a-1753-4d39-a562-b9d274d9946412016-09-02
43063-693-90EA - Each43063-693f3123e91-3724-4de1-a92f-8ebb041e6e5812016-09-02
43063-693-93EA - Each43063-6931d630492-9320-47f9-a8df-89509458628e12016-09-02