naproxen
Generic: naproxen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
naproxen
Generic Name
naproxen
Labeler
proficient rx lp
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
naproxen 375 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-060
Product ID
71205-060_6b4c9ec2-308f-4b60-941c-34a2c7a7882c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091432
Listing Expiration
2026-12-31
Marketing Start
2016-07-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205060
Hyphenated Format
71205-060
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
ANDA091432 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 375 mg/1
Packaging
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-14)
- 15 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-15)
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-20)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-30)
- 40 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-40)
- 45 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-45)
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-60)
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-90)
Packages (8)
71205-060-14
14 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-14)
71205-060-15
15 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-15)
71205-060-20
20 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-20)
71205-060-30
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-30)
71205-060-40
40 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-40)
71205-060-45
45 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-45)
71205-060-60
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-60)
71205-060-90
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6b4c9ec2-308f-4b60-941c-34a2c7a7882c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["603103"], "spl_set_id": ["69a3afd6-d64b-4f07-b848-b0d3fc19f2a2"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-14)", "package_ndc": "71205-060-14", "marketing_start_date": "20180601"}, {"sample": false, "description": "15 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-15)", "package_ndc": "71205-060-15", "marketing_start_date": "20180601"}, {"sample": false, "description": "20 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-20)", "package_ndc": "71205-060-20", "marketing_start_date": "20180601"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-30)", "package_ndc": "71205-060-30", "marketing_start_date": "20180601"}, {"sample": false, "description": "40 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-40)", "package_ndc": "71205-060-40", "marketing_start_date": "20180601"}, {"sample": false, "description": "45 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-45)", "package_ndc": "71205-060-45", "marketing_start_date": "20180601"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-60)", "package_ndc": "71205-060-60", "marketing_start_date": "20180601"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-90)", "package_ndc": "71205-060-90", "marketing_start_date": "20180601"}], "brand_name": "Naproxen", "product_id": "71205-060_6b4c9ec2-308f-4b60-941c-34a2c7a7882c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-060", "generic_name": "Naproxen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "375 mg/1"}], "application_number": "ANDA091432", "marketing_category": "ANDA", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}