naproxen

Generic: naproxen

Labeler: time cap laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen
Labeler time cap laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen 375 mg/1

Manufacturer
TIME CAP LABORATORIES

Identifiers & Regulatory

Product NDC 49483-617
Product ID 49483-617_77d2030d-4699-2117-e053-2a91aa0a6dc8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091416
Listing Expiration 2026-12-31
Marketing Start 2016-07-06

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 49483617
Hyphenated Format 49483-617

Supplemental Identifiers

RxCUI
198012 198013 198014
UPC
0349483617016 0349483618013 0349483619010
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 ANDA091416 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 375 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (49483-617-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (49483-617-50)
source: ndc

Packages (2)

Ingredients (1)

naproxen (375 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77d2030d-4699-2117-e053-2a91aa0a6dc8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483617016", "0349483618013", "0349483619010"], "unii": ["57Y76R9ATQ"], "rxcui": ["198012", "198013", "198014"], "spl_set_id": ["4350a2d9-5228-460e-b7b1-27e8fa846787"], "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": ["TIME CAP LABORATORIES"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (49483-617-01)", "package_ndc": "49483-617-01", "marketing_start_date": "20160706"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (49483-617-50)", "package_ndc": "49483-617-50", "marketing_start_date": "20160706"}], "brand_name": "NAPROXEN", "product_id": "49483-617_77d2030d-4699-2117-e053-2a91aa0a6dc8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-617", "generic_name": "NAPROXEN", "labeler_name": "TIME CAP LABORATORIES", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAPROXEN", "active_ingredients": [{"name": "NAPROXEN", "strength": "375 mg/1"}], "application_number": "ANDA091416", "marketing_category": "ANDA", "marketing_start_date": "20160706", "listing_expiration_date": "20261231"}