Package 68788-7800-6

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7800-6
Digits Only 6878878006
Product NDC 68788-7800
Description

60 TABLET in 1 BOTTLE (68788-7800-6)

Marketing

Marketing Status
Marketed Since 2020-10-13
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e522f024-b4ac-4ff4-8368-e9e6da9eb37e", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["6ae413ba-5a48-423f-8b8d-7a42661cf836"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7800-1)", "package_ndc": "68788-7800-1", "marketing_start_date": "20201013"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7800-2)", "package_ndc": "68788-7800-2", "marketing_start_date": "20201013"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7800-3)", "package_ndc": "68788-7800-3", "marketing_start_date": "20201013"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-7800-4)", "package_ndc": "68788-7800-4", "marketing_start_date": "20201013"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7800-6)", "package_ndc": "68788-7800-6", "marketing_start_date": "20201013"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-7800-8)", "package_ndc": "68788-7800-8", "marketing_start_date": "20201013"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7800-9)", "package_ndc": "68788-7800-9", "marketing_start_date": "20201013"}], "brand_name": "Naproxen Sodium", "product_id": "68788-7800_e522f024-b4ac-4ff4-8368-e9e6da9eb37e", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7800", "generic_name": "Naproxen Sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA212199", "marketing_category": "ANDA", "marketing_start_date": "20201013", "listing_expiration_date": "20261231"}