naproxen

Generic: naproxen

Labeler: zameer pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen
Labeler zameer pharmaceuticals llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

naproxen 500 mg/1

Manufacturer
Zameer Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 90096-161
Product ID 90096-161_1e574b03-a038-453b-b84f-9437fc2df0f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020067
Listing Expiration 2026-12-31
Marketing Start 2025-08-31

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 90096161
Hyphenated Format 90096-161

Supplemental Identifiers

RxCUI
311915
UNII
57Y76R9ATQ
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 NDA020067 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01)
source: ndc

Packages (1)

Ingredients (1)

naproxen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1e574b03-a038-453b-b84f-9437fc2df0f8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915"], "spl_set_id": ["d2e5553a-7c90-407c-9f07-3be65560c23a"], "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": ["Zameer Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01)", "package_ndc": "90096-161-01", "marketing_start_date": "20250831"}], "brand_name": "Naproxen", "product_id": "90096-161_1e574b03-a038-453b-b84f-9437fc2df0f8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "90096-161", "generic_name": "Naproxen", "labeler_name": "Zameer Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "NDA020067", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250831", "listing_expiration_date": "20261231"}