Package 69452-179-22
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
69452-179-22
Digits Only
6945217922
Product NDC
69452-179
Description
120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-179-22)
Marketing
Marketing Status
Brand
naproxen sodium
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d85dc59-4954-47fc-e063-6394a90a01cd", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["1112231"], "spl_set_id": ["3e10256f-0a5f-49e4-9518-a72b10490f89"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-179-22)", "package_ndc": "69452-179-22", "marketing_start_date": "20181101"}], "brand_name": "Naproxen Sodium", "product_id": "69452-179_0d85dc59-4954-47fc-e063-6394a90a01cd", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69452-179", "generic_name": "Naproxen Sodium", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "NDA021920", "marketing_category": "NDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}