pain relief

Generic: naproxen sodium

Labeler: gobrands, inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name naproxen sodium
Labeler gobrands, inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Gobrands, Inc

Identifiers & Regulatory

Product NDC 82501-1576
Product ID 82501-1576_29ba15a4-8de5-e97f-e063-6394a90a6c9a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091353
Listing Expiration 2026-12-31
Marketing Start 2022-05-30

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 825011576
Hyphenated Format 82501-1576

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

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 pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA091353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)
source: ndc

Packages (1)

82501-1576-1 100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29ba15a4-8de5-e97f-e063-6394a90a6c9a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["ae4bfa8c-ae41-4fcd-b584-872cc4d37683"], "manufacturer_name": ["Gobrands, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (82501-1576-1)", "package_ndc": "82501-1576-1", "marketing_start_date": "20220530"}], "brand_name": "Pain Relief", "product_id": "82501-1576_29ba15a4-8de5-e97f-e063-6394a90a6c9a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82501-1576", "generic_name": "Naproxen Sodium", "labeler_name": "Gobrands, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20220530", "listing_expiration_date": "20261231"}