Diclofenac sodium

Product NDC

68071-3159

11-digit product format

680713159

Labeler code

68071

Product ID

68071-3159_4adc8290-1687-4b3f-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac

Dosage form

GEL

Route

TOPICAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA208077

Marketing category

ANDA

Marketing start

2016-03-21

Marketing end

0000-00-00

Substance

DICLOFENAC SODIUM

Active strength

10 mg/g

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