naproxen sodium

Generic: naproxen sodium

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 550 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7800
Product ID 68788-7800_e522f024-b4ac-4ff4-8368-e9e6da9eb37e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212199
Listing Expiration 2026-12-31
Marketing Start 2020-10-13

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 687887800
Hyphenated Format 68788-7800

Supplemental Identifiers

RxCUI
849431
UNII
9TN87S3A3C

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 sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA212199 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 550 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7800-1)
  • 20 TABLET in 1 BOTTLE (68788-7800-2)
  • 30 TABLET in 1 BOTTLE (68788-7800-3)
  • 14 TABLET in 1 BOTTLE (68788-7800-4)
  • 60 TABLET in 1 BOTTLE (68788-7800-6)
  • 120 TABLET in 1 BOTTLE (68788-7800-8)
  • 90 TABLET in 1 BOTTLE (68788-7800-9)
source: ndc

Packages (7)

Ingredients (1)

naproxen sodium (550 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e522f024-b4ac-4ff4-8368-e9e6da9eb37e", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["6ae413ba-5a48-423f-8b8d-7a42661cf836"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7800-1)", "package_ndc": "68788-7800-1", "marketing_start_date": "20201013"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7800-2)", "package_ndc": "68788-7800-2", "marketing_start_date": "20201013"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7800-3)", "package_ndc": "68788-7800-3", "marketing_start_date": "20201013"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-7800-4)", "package_ndc": "68788-7800-4", "marketing_start_date": "20201013"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7800-6)", "package_ndc": "68788-7800-6", "marketing_start_date": "20201013"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-7800-8)", "package_ndc": "68788-7800-8", "marketing_start_date": "20201013"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7800-9)", "package_ndc": "68788-7800-9", "marketing_start_date": "20201013"}], "brand_name": "Naproxen Sodium", "product_id": "68788-7800_e522f024-b4ac-4ff4-8368-e9e6da9eb37e", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7800", "generic_name": "Naproxen Sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA212199", "marketing_category": "ANDA", "marketing_start_date": "20201013", "listing_expiration_date": "20261231"}