naproxen

Generic: naproxen

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen 375 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-650
Product ID 43063-650_39f9273f-87db-b615-e063-6294a90a03b6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075927
Listing Expiration 2026-12-31
Marketing Start 2010-02-18

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 43063650
Hyphenated Format 43063-650

Supplemental Identifiers

RxCUI
198012
UPC
0343063650202
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 ANDA075927 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 375 mg/1
source: ndc
Packaging
  • 6 TABLET in 1 BOTTLE, PLASTIC (43063-650-06)
  • 10 TABLET in 1 BOTTLE, PLASTIC (43063-650-10)
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-650-14)
  • 15 TABLET in 1 BOTTLE, PLASTIC (43063-650-15)
  • 20 TABLET in 1 BOTTLE, PLASTIC (43063-650-20)
  • 21 TABLET in 1 BOTTLE, PLASTIC (43063-650-21)
  • 24 TABLET in 1 BOTTLE, PLASTIC (43063-650-24)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-650-30)
  • 42 TABLET in 1 BOTTLE, PLASTIC (43063-650-42)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-650-60)
source: ndc

Packages (10)

Ingredients (1)

naproxen (375 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39f9273f-87db-b615-e063-6294a90a03b6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0343063650202"], "unii": ["57Y76R9ATQ"], "rxcui": ["198012"], "spl_set_id": ["29d98cf3-a0f2-3f89-e054-00144ff88e88"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-650-06)", "package_ndc": "43063-650-06", "marketing_start_date": "20160122"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43063-650-10)", "package_ndc": "43063-650-10", "marketing_start_date": "20160122"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-650-14)", "package_ndc": "43063-650-14", "marketing_start_date": "20160122"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (43063-650-15)", "package_ndc": "43063-650-15", "marketing_start_date": "20160122"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (43063-650-20)", "package_ndc": "43063-650-20", "marketing_start_date": "20160122"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (43063-650-21)", "package_ndc": "43063-650-21", "marketing_start_date": "20160122"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE, PLASTIC (43063-650-24)", "package_ndc": "43063-650-24", "marketing_start_date": "20160122"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-650-30)", "package_ndc": "43063-650-30", "marketing_start_date": "20160122"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (43063-650-42)", "package_ndc": "43063-650-42", "marketing_start_date": "20160122"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-650-60)", "package_ndc": "43063-650-60", "marketing_start_date": "20160122"}], "brand_name": "Naproxen", "product_id": "43063-650_39f9273f-87db-b615-e063-6294a90a03b6", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-650", "generic_name": "Naproxen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "375 mg/1"}], "application_number": "ANDA075927", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}