Diclofenac Sodium

Product NDC
43063-694
11-digit product format
430630694
Labeler code
43063
Product ID
43063-694_7d4f9885-3e9a-bd28-e053-2a91aa0a0392
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
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
43063-694-60EA - Each43063-694697472a8-fff6-466f-8974-3b083cf20b3412016-09-02
43063-694-90EA - Each43063-694a9d99815-25e3-4d7a-ade5-ff7e22f9345112016-09-02
43063-694-93EA - Each43063-6948006cbfd-058c-4d60-9cb2-d2fbb10ed79b12016-09-02