Package 50090-7856-0

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7856-0
Digits Only 5009078560
Product NDC 50090-7856
Product ID 50090-7856_61c6cba8-e4f2-4222-9db3-cf97c67b4dec
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7856-0)

Marketing

Marketing Status
Marketed Since 2026-01-14
Brand diclofenac sodium
Generic diclofenac sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "61c6cba8-e4f2-4222-9db3-cf97c67b4dec", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["f92576d7-3ad9-43a3-8b10-3a29fbf712a4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7856-0)", "package_ndc": "50090-7856-0", "marketing_start_date": "20260114"}], "brand_name": "DICLOFENAC SODIUM", "product_id": "50090-7856_61c6cba8-e4f2-4222-9db3-cf97c67b4dec", "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": "50090-7856", "generic_name": "DICLOFENAC SODIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOFENAC SODIUM", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075281", "marketing_category": "ANDA", "marketing_start_date": "20250417", "listing_expiration_date": "20271231"}