naproxen sodium
Generic: naproxen sodium
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
naproxen sodium
Generic Name
naproxen sodium
Labeler
preferred pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
naproxen sodium 550 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887800
Hyphenated Format
68788-7800
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 550 mg/1
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)
Packages (7)
68788-7800-1
100 TABLET in 1 BOTTLE (68788-7800-1)
68788-7800-2
20 TABLET in 1 BOTTLE (68788-7800-2)
68788-7800-3
30 TABLET in 1 BOTTLE (68788-7800-3)
68788-7800-4
14 TABLET in 1 BOTTLE (68788-7800-4)
68788-7800-6
60 TABLET in 1 BOTTLE (68788-7800-6)
68788-7800-8
120 TABLET in 1 BOTTLE (68788-7800-8)
68788-7800-9
90 TABLET in 1 BOTTLE (68788-7800-9)
Ingredients (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"}