Package 60687-658-01
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
60687-658-01
Digits Only
6068765801
Product NDC
60687-658
Description
100 BLISTER PACK in 1 CARTON (60687-658-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-658-11)
Marketing
Marketing Status
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": "3d815bff-1a72-6901-e063-6394a90a127d", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["dbb1489d-b690-4e53-905d-7fb07ad263b3"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-658-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-658-11)", "package_ndc": "60687-658-01", "marketing_start_date": "20220822"}], "brand_name": "Diclofenac Sodium", "product_id": "60687-658_3d815bff-1a72-6901-e063-6394a90a127d", "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": "60687-658", "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": "75 mg/1"}], "application_number": "ANDA077863", "marketing_category": "ANDA", "marketing_start_date": "20220822", "listing_expiration_date": "20261231"}