naproxen
Generic: naproxen
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
naproxen
Generic Name
naproxen
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
naproxen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8602
Product ID
68788-8602_f6aaf43d-d2fe-45a6-b984-e3909c5e75de
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212517
Listing Expiration
2026-12-31
Marketing Start
2024-04-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888602
Hyphenated Format
68788-8602
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
naproxen (source: ndc)
Generic Name
naproxen (source: ndc)
Application Number
ANDA212517 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68788-8602-1)
- 20 TABLET in 1 BOTTLE (68788-8602-2)
- 30 TABLET in 1 BOTTLE (68788-8602-3)
- 40 TABLET in 1 BOTTLE (68788-8602-4)
- 15 TABLET in 1 BOTTLE (68788-8602-5)
- 60 TABLET in 1 BOTTLE (68788-8602-6)
- 14 TABLET in 1 BOTTLE (68788-8602-7)
- 120 TABLET in 1 BOTTLE (68788-8602-8)
- 90 TABLET in 1 BOTTLE (68788-8602-9)
Packages (9)
68788-8602-1
100 TABLET in 1 BOTTLE (68788-8602-1)
68788-8602-2
20 TABLET in 1 BOTTLE (68788-8602-2)
68788-8602-3
30 TABLET in 1 BOTTLE (68788-8602-3)
68788-8602-4
40 TABLET in 1 BOTTLE (68788-8602-4)
68788-8602-5
15 TABLET in 1 BOTTLE (68788-8602-5)
68788-8602-6
60 TABLET in 1 BOTTLE (68788-8602-6)
68788-8602-7
14 TABLET in 1 BOTTLE (68788-8602-7)
68788-8602-8
120 TABLET in 1 BOTTLE (68788-8602-8)
68788-8602-9
90 TABLET in 1 BOTTLE (68788-8602-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6aaf43d-d2fe-45a6-b984-e3909c5e75de", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["49a00870-f580-4eb9-a95d-48fa956f147f"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8602-1)", "package_ndc": "68788-8602-1", "marketing_start_date": "20240401"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8602-2)", "package_ndc": "68788-8602-2", "marketing_start_date": "20240401"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8602-3)", "package_ndc": "68788-8602-3", "marketing_start_date": "20240401"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68788-8602-4)", "package_ndc": "68788-8602-4", "marketing_start_date": "20240401"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8602-5)", "package_ndc": "68788-8602-5", "marketing_start_date": "20240401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8602-6)", "package_ndc": "68788-8602-6", "marketing_start_date": "20240401"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-8602-7)", "package_ndc": "68788-8602-7", "marketing_start_date": "20240401"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-8602-8)", "package_ndc": "68788-8602-8", "marketing_start_date": "20240401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8602-9)", "package_ndc": "68788-8602-9", "marketing_start_date": "20240401"}], "brand_name": "Naproxen", "product_id": "68788-8602_f6aaf43d-d2fe-45a6-b984-e3909c5e75de", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8602", "generic_name": "Naproxen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA212517", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}