Package 71993-312-30

Brand: tolmetin sodium

Generic: tolmetin sodium
NDC Package

Package Facts

Identity

Package NDC 71993-312-30
Digits Only 7199331230
Product NDC 71993-312
Product ID 71993-312_24ffd8d5-f836-4914-b4d9-1cc420e01fa3
Description

30 TABLET, FILM COATED in 1 BOTTLE (71993-312-30)

Marketing

Marketing Status
Marketed Since 2025-02-25
Brand tolmetin sodium
Generic tolmetin sodium
Sample Package No

Linked Drug Pages (1)

Tolmetin Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24ffd8d5-f836-4914-b4d9-1cc420e01fa3", "openfda": {"upc": ["0371993312303"], "unii": ["02N1TZF99F"], "rxcui": ["198297"], "spl_set_id": ["e6150446-c5ef-4437-b488-067876649fcc"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71993-312-30)", "package_ndc": "71993-312-30", "marketing_start_date": "20250225"}], "brand_name": "Tolmetin Sodium", "product_id": "71993-312_24ffd8d5-f836-4914-b4d9-1cc420e01fa3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71993-312", "generic_name": "Tolmetin Sodium", "labeler_name": "Atland Pharmaceuticals, LLC", "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_start_date": "20250225", "listing_expiration_date": "20261231"}