Package 50991-988-30

Brand: tolectin

Generic: tolmetin sodium
NDC Package

Package Facts

Identity

Package NDC 50991-988-30
Digits Only 5099198830
Product NDC 50991-988
Description

30 TABLET, FILM COATED in 1 BOTTLE (50991-988-30)

Marketing

Marketing Status
Marketed Since 2024-04-04
Brand tolectin
Generic tolmetin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472dd96d-50bb-e82c-e063-6294a90af66d", "openfda": {"upc": ["0350991988307"], "unii": ["02N1TZF99F"], "rxcui": ["198297", "208048"], "spl_set_id": ["15467b19-e43a-5be9-e063-6294a90a3cca"], "manufacturer_name": ["Poly Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50991-988-30)", "package_ndc": "50991-988-30", "marketing_start_date": "20240404"}], "brand_name": "Tolectin", "product_id": "50991-988_472dd96d-50bb-e82c-e063-6294a90af66d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50991-988", "generic_name": "tolmetin sodium", "labeler_name": "Poly Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolectin", "active_ingredients": [{"name": "TOLMETIN SODIUM", "strength": "600 mg/1"}], "application_number": "ANDA074473", "marketing_category": "ANDA", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}