Package 63629-2010-1

Brand: diclofenac sodium delayed release

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 63629-2010-1
Digits Only 6362920101
Product NDC 63629-2010
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63629-2010-1)

Marketing

Marketing Status
Marketed Since 2021-02-16
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": "84b0a694-8ea3-4cb8-a161-a3c9921d7d65", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["2bebda5e-227e-4a49-80e3-191cfc805295"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63629-2010-1)", "package_ndc": "63629-2010-1", "marketing_start_date": "20210216"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "63629-2010_84b0a694-8ea3-4cb8-a161-a3c9921d7d65", "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": "63629-2010", "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": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}