Package 36800-140-82

Brand: topcare all day pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 36800-140-82
Digits Only 3680014082
Product NDC 36800-140
Description

200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82)

Marketing

Marketing Status
Marketed Since 2007-12-03
Brand topcare all day pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9e77ead9-aabd-4ce0-a89d-86dd168c2663", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f151d48d-a8f7-484e-9ce8-6b2e8dd1093f"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82)", "package_ndc": "36800-140-82", "marketing_start_date": "20071203"}], "brand_name": "Topcare All Day Pain Relief", "product_id": "36800-140_9e77ead9-aabd-4ce0-a89d-86dd168c2663", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "36800-140", "generic_name": "Naproxen sodium", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Topcare All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20071203", "listing_expiration_date": "20261231"}