Package 63629-2012-1
Brand: diclofenac sodium delayed release
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
63629-2012-1
Digits Only
6362920121
Product NDC
63629-2012
Description
12 BOTTLE, PLASTIC in 1 BOX (63629-2012-1) / 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
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": "9f005ea7-9f4a-4c7f-8e21-74de2dc49ece", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["bced0ef0-085a-40db-9678-2bc6eb77d456"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "12 BOTTLE, PLASTIC in 1 BOX (63629-2012-1) / 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "63629-2012-1", "marketing_start_date": "19981113"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "63629-2012_9f005ea7-9f4a-4c7f-8e21-74de2dc49ece", "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": "63629-2012", "generic_name": "Diclofenac Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}