Package 60687-606-01

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 60687-606-01
Digits Only 6068760601
Product NDC 60687-606
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-606-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-606-11)

Marketing

Marketing Status
Marketed Since 2022-06-07
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2f22d370-066e-50d8-e063-6394a90a110a", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["63c00b50-06d3-4659-81cf-be4516429e81"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-606-01)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-606-11)", "package_ndc": "60687-606-01", "marketing_start_date": "20220607"}], "brand_name": "Diclofenac Sodium", "product_id": "60687-606_2f22d370-066e-50d8-e063-6394a90a110a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "60687-606", "generic_name": "Diclofenac Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA090066", "marketing_category": "ANDA", "marketing_start_date": "20220607", "listing_expiration_date": "20261231"}