Package 43598-059-52
Brand: naproxen sodium headache pain caplets
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
43598-059-52
Digits Only
4359805952
Product NDC
43598-059
Description
225 TABLET, COATED in 1 BOTTLE (43598-059-52)
Marketing
Marketing Status
Brand
naproxen sodium headache pain caplets
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7f658fac-fde0-3b5d-f8ad-15dcaf71cdad", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["605ca130-88aa-27d5-330c-6d9c95987f1f"], "manufacturer_name": ["Dr.Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE (43598-059-52)", "package_ndc": "43598-059-52", "marketing_start_date": "20210805"}], "brand_name": "Naproxen Sodium Headache Pain Caplets", "product_id": "43598-059_7f658fac-fde0-3b5d-f8ad-15dcaf71cdad", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43598-059", "generic_name": "Naproxen Sodium", "labeler_name": "Dr.Reddy's Laboratories Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "brand_name_suffix": "Headache Pain Caplets", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA075168", "marketing_category": "ANDA", "marketing_start_date": "20210805", "listing_expiration_date": "20261231"}