naproxen

Generic: naproxen

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen 375 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-535
Product ID 63187-535_bd0691c5-aaa9-472e-9b05-926d93defd0c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078250
Listing Expiration 2026-12-31
Marketing Start 2007-07-01

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187535
Hyphenated Format 63187-535

Supplemental Identifiers

RxCUI
198012
UNII
57Y76R9ATQ
NUI
N0000000160 M0001335 N0000175722

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 ANDA078250 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 375 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (63187-535-15)
  • 20 TABLET in 1 BOTTLE (63187-535-20)
  • 30 TABLET in 1 BOTTLE (63187-535-30)
  • 45 TABLET in 1 BOTTLE (63187-535-45)
  • 60 TABLET in 1 BOTTLE (63187-535-60)
  • 90 TABLET in 1 BOTTLE (63187-535-90)
source: ndc

Packages (6)

63187-535-15 15 TABLET in 1 BOTTLE (63187-535-15) 63187-535-20 20 TABLET in 1 BOTTLE (63187-535-20) 63187-535-30 30 TABLET in 1 BOTTLE (63187-535-30) 63187-535-45 45 TABLET in 1 BOTTLE (63187-535-45) 63187-535-60 60 TABLET in 1 BOTTLE (63187-535-60) 63187-535-90 90 TABLET in 1 BOTTLE (63187-535-90)

Ingredients (1)

naproxen (375 mg/1)

Linked Drug Pages (1)

Naproxen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bd0691c5-aaa9-472e-9b05-926d93defd0c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198012"], "spl_set_id": ["3e4e5371-d796-47c7-95c1-d99e82a0b282"], "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": "15 TABLET in 1 BOTTLE (63187-535-15)", "package_ndc": "63187-535-15", "marketing_start_date": "20181201"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-535-20)", "package_ndc": "63187-535-20", "marketing_start_date": "20181201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-535-30)", "package_ndc": "63187-535-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (63187-535-45)", "package_ndc": "63187-535-45", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-535-60)", "package_ndc": "63187-535-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-535-90)", "package_ndc": "63187-535-90", "marketing_start_date": "20181201"}], "brand_name": "Naproxen", "product_id": "63187-535_bd0691c5-aaa9-472e-9b05-926d93defd0c", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-535", "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": "ANDA078250", "marketing_category": "ANDA", "marketing_start_date": "20070701", "listing_expiration_date": "20261231"}