naproxen

Generic: naproxen sodium

Labeler: family dollar services inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen sodium
Labeler family dollar services inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Family Dollar Services Inc

Identifiers & Regulatory

Product NDC 55319-717
Product ID 55319-717_44293b70-2dbb-442c-945d-efb1f54b87fc
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Listing Expiration 2026-12-31
Marketing Start 2023-12-13

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 55319717
Hyphenated Format 55319-717

Supplemental Identifiers

RxCUI
849574
UPC
0032251923784
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 naproxen (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (55319-717-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44293b70-2dbb-442c-945d-efb1f54b87fc", "openfda": {"upc": ["0032251923784"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b6205032-f5c6-494a-8b87-adbbbc3982e7"], "manufacturer_name": ["Family Dollar Services Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (55319-717-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "55319-717-08", "marketing_start_date": "20231213"}], "brand_name": "Naproxen", "product_id": "55319-717_44293b70-2dbb-442c-945d-efb1f54b87fc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55319-717", "generic_name": "Naproxen Sodium", "labeler_name": "Family Dollar Services Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20231213", "listing_expiration_date": "20261231"}