Diclofenac Sodium

Product NDC

70518-0851

11-digit product format

705180851

Labeler code

70518

Product ID

70518-0851_5e0f0cca-20c5-382d-e053-2991aa0a5b17

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diclofenac Sodium

Dosage form

GEL

Route

TOPICAL

Labeler

REMEDYREPACK INC.

Application

ANDA200936

Marketing category

ANDA

Marketing start

2017-11-15

Marketing end

0000-00-00

Substance

DICLOFENAC SODIUM

Active strength

30 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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record