naproxen
Generic: naproxen
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
naproxen
Generic Name
naproxen
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
naproxen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4006
Product ID
68071-4006_1d7a3c9a-73d5-5360-e063-6394a90aa3e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091416
Listing Expiration
2026-12-31
Marketing Start
2016-07-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714006
Hyphenated Format
68071-4006
Supplemental Identifiers
RxCUI
UPC
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
ANDA091416 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (68071-4006-1)
- 20 TABLET in 1 BOTTLE (68071-4006-2)
- 30 TABLET in 1 BOTTLE (68071-4006-3)
- 40 TABLET in 1 BOTTLE (68071-4006-4)
- 15 TABLET in 1 BOTTLE (68071-4006-5)
- 60 TABLET in 1 BOTTLE (68071-4006-6)
- 14 TABLET in 1 BOTTLE (68071-4006-7)
- 90 TABLET in 1 BOTTLE (68071-4006-9)
Packages (8)
68071-4006-1
10 TABLET in 1 BOTTLE (68071-4006-1)
68071-4006-2
20 TABLET in 1 BOTTLE (68071-4006-2)
68071-4006-3
30 TABLET in 1 BOTTLE (68071-4006-3)
68071-4006-4
40 TABLET in 1 BOTTLE (68071-4006-4)
68071-4006-5
15 TABLET in 1 BOTTLE (68071-4006-5)
68071-4006-6
60 TABLET in 1 BOTTLE (68071-4006-6)
68071-4006-7
14 TABLET in 1 BOTTLE (68071-4006-7)
68071-4006-9
90 TABLET in 1 BOTTLE (68071-4006-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d7a3c9a-73d5-5360-e063-6394a90aa3e6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071400625"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["5487dee2-5c37-4348-e054-00144ff8d46c"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4006-1)", "package_ndc": "68071-4006-1", "marketing_start_date": "20170717"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4006-2)", "package_ndc": "68071-4006-2", "marketing_start_date": "20170717"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4006-3)", "package_ndc": "68071-4006-3", "marketing_start_date": "20170717"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68071-4006-4)", "package_ndc": "68071-4006-4", "marketing_start_date": "20170717"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68071-4006-5)", "package_ndc": "68071-4006-5", "marketing_start_date": "20170717"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4006-6)", "package_ndc": "68071-4006-6", "marketing_start_date": "20170717"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-4006-7)", "package_ndc": "68071-4006-7", "marketing_start_date": "20170717"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-4006-9)", "package_ndc": "68071-4006-9", "marketing_start_date": "20170717"}], "brand_name": "NAPROXEN", "product_id": "68071-4006_1d7a3c9a-73d5-5360-e063-6394a90aa3e6", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-4006", "generic_name": "NAPROXEN", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAPROXEN", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA091416", "marketing_category": "ANDA", "marketing_start_date": "20160706", "listing_expiration_date": "20261231"}