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NDC 70934-0678-30 Diclofenac Sodium 75 mg/1 Details

Diclofenac Sodium 75 mg/1

Diclofenac Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is DICLOFENAC SODIUM.

MedlinePlus Drug Summary

Diclofenac capsules (Zipsor, Zorvolex) and tablets (Cataflam) are used to relieve mild to moderate pain. Diclofenac extended-release tablets (Voltaren XR), tablets (Cataflam), and delayed-release tablets (available generically) are used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints), and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Diclofenac extended-release tablets and delayed-release tablets are also used to treat ankylosing spondylitis (arthritis that mainly affects the spine). Diclofenac tablets (Cataflam) are also used to treat painful menstrual periods. Diclofenac solution (Cambia) is used to treat migraine headaches in adults, but cannot be used to prevent migraines or to treat other types of headaches. Diclofenac is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 70934-0678-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Diclofenac

Product Information

NDC	70934-0678
Product ID	70934-678_f18537c2-e417-e1ec-e053-2a95a90a0d7c
Associated GPIs	66100007200630
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Diclofenac Sodium
Proprietary Name Suffix	Delayed Release
Non-Proprietary Name	Diclofenac Sodium
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, DELAYED RELEASE
Route	ORAL
Active Ingredient Strength	75
Active Ingredient Units	mg/1
Substance Name	DICLOFENAC SODIUM
Labeler Name	Denton Pharma, Inc. dba Northwind Pharmaceuticals
Pharmaceutical Class	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA075185
Listing Certified Through	n/a

Package

NDC 70934-0678-30 (70934067830)

Pricing Information	N/A
NDC Package Code	70934-678-30
Billing NDC	70934067830
Package	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-678-30)
Marketing Start Date	2020-04-22
NDC Exclude Flag	N