Package 16571-825-09

Brand: tolmetin sodium

Generic: tolmetin sodium
NDC Package

Package Facts

Identity

Package NDC 16571-825-09
Digits Only 1657182509
Product NDC 16571-825
Description

90 TABLET, FILM COATED in 1 BOTTLE (16571-825-09)

Marketing

Marketing Status
Discontinued 2026-05-31
Brand tolmetin sodium
Generic tolmetin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff84bf16-f778-489c-9cb0-c6df96b5b56d", "openfda": {"upc": ["0316571825097"], "unii": ["02N1TZF99F"], "rxcui": ["198297"], "spl_set_id": ["fa4096f0-0d22-4421-b4ca-6b1d7f078bd3"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16571-825-09)", "package_ndc": "16571-825-09", "marketing_end_date": "20260531", "marketing_start_date": "20230411"}], "brand_name": "TOLMETIN SODIUM", "product_id": "16571-825_ff84bf16-f778-489c-9cb0-c6df96b5b56d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "16571-825", "generic_name": "tolmetin sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TOLMETIN SODIUM", "active_ingredients": [{"name": "TOLMETIN SODIUM", "strength": "600 mg/1"}], "application_number": "ANDA074473", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20230411"}