Package 70518-0756-0
Brand: diclofenac sodium delayed release
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
70518-0756-0
Digits Only
7051807560
Product NDC
70518-0756
Description
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0756-0)
Marketing
Marketing Status
Brand
diclofenac sodium delayed release
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4833cde3-82a4-dd82-e063-6394a90a63a4", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["14c1b1a1-bc06-4722-9612-e88ae52272bc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0756-0)", "package_ndc": "70518-0756-0", "marketing_start_date": "20171004"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "70518-0756_4833cde3-82a4-dd82-e063-6394a90a63a4", "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": "70518-0756", "generic_name": "Diclofenac Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20271231"}