ec-naproxen

Generic: naproxen

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ec-naproxen
Generic Name naproxen
Labeler bryant ranch prepack
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

naproxen 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1935
Product ID 72162-1935_4ce24976-cf2a-419a-82fd-1ef1efb0c031
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020067
Listing Expiration 2026-12-31
Marketing Start 2018-10-15

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 721621935
Hyphenated Format 72162-1935

Supplemental Identifiers

RxCUI
311915
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 ec-naproxen (source: ndc)
Generic Name naproxen (source: ndc)
Application Number NDA020067 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1935-1)
source: ndc

Packages (1)

72162-1935-1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1935-1)

Ingredients (1)

naproxen (500 mg/1)

Linked Drug Pages (1)

EC-NAPROXEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4ce24976-cf2a-419a-82fd-1ef1efb0c031", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915"], "spl_set_id": ["7199cf50-68e6-460f-9832-183d4678d1e8"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1935-1)", "package_ndc": "72162-1935-1", "marketing_start_date": "20240530"}], "brand_name": "EC-NAPROXEN", "product_id": "72162-1935_4ce24976-cf2a-419a-82fd-1ef1efb0c031", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72162-1935", "generic_name": "naproxen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EC-NAPROXEN", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "NDA020067", "marketing_category": "NDA", "marketing_start_date": "20181015", "listing_expiration_date": "20261231"}